Synthesis, Characterization and Cytotoxicity Studies of Aminated Microcrystalline Cellulose Derivatives against Melanoma and Breast Cancer Cell Lines

Cellulose based materials are emerging in the commercial fields and high-end applications, especially in biomedicines. Aminated cellulose derivatives have been extensively used for various applications but limited data are available regarding its cytotoxicity studies for biomedical application. The aim of this study is to synthesize different 6-deoxy-amino-cellulose derivatives from Microcrystalline cellulose (MCC) via tosylation and explore their cytotoxic potential against normal fibroblasts, melanoma and breast cancer. 6-deoxy-6-hydrazide Cellulose (Cell Hyd) 6-deoxy-6-diethylamide Cellulose (Cell DEA) and 6-deoxy-6-diethyltriamine Cellulose (Cell DETA) were prepared and characterized by various technologies like Fourier transform infrared spectroscopy-attenuated total reflectance (FTIR-ATR), nuclear magnetic resonance spectroscopy (NMR), X-ray diffractogram (XRD), Scanning Electron microscopy (SEM), Elemental Analysis and Zeta potential measurements. Cytotoxicity was evaluated against normal fibroblasts (NIH3T3), mouse skin melanoma (B16F10), human epithelial adenocarcinoma (MDA-MB-231) and human breast adenocarcinoma (MCF-7) cell lines. IC50 values obtained from cytotoxicity assay and live/dead assay images analysis showed MCC was non cytotoxic while Cell Hyd, Cell DEA and Cell DETA exhibited noncytotoxic activity up to 200 μg/mL to normal fibroblast cells NIH3T3, suggesting its safe use in medical fields. The mouse skin melanoma (B16F10) are the most sensitive cells to the cytotoxic effects of Cell Hyd, Cell DEA and Cell DETA, followed by human breast adenocarcinoma (MCF-7). Based on our study, it is suggested that aminated cellulose derivatives could be promising candidates for tissue engineering applications and in cancer inhibiting studies in future.


Introduction
Cancer is the uncontrolled cell division of abnormal cells clinically known as the malignant tumor or malignant neoplasm. Cancer is the second deadliest disease after heart disease, resulting in five hundred and fifty thousand deaths per year, 7.6 million in 2008 and expected to be 13.1 million by 2030 [1]. At present, drug resistance, side effects like systemic toxicity, high mortality rate and high costs [2] limit many cutting edge researches and chemotherapeutics. The medicinal chemistry field is always looking for the development of new anticancer therapeutics with lower toxicity and high efficiency [1].
Polymeric materials from renewable resources are widely used in medical, food, agriculture, biomedicinal and environmental studies. Natural polymers such as polysaccharides play the most efficient role in biomedical product preparation. Polysaccharides have wide molecular weight range and good number of functional groups for suitable chemical modification. Polysaccharides positively lation of Cellulose microcrystalline Cellulose MCC, 10 g (61.6 mM of anhydrous glucose unit (AGU)) was 00 mL flask, and 250 mL of N,N-Dimethyl acetamide synthetic grade (DMA) was added at 120 °C for 1 h. Resulting slurry was cooled to 100 °C, and then, Lithium Chloride s LiCl, (20 g) in DMA (50 mL), was added dropwise. Stirring was continued overnight until te dissolution of the Cellulose. A volume of 37.2 mL of Triethylamine (TEA) (370 mM), 6 in 20 mL of DMA, was added to the cellulose solution at constant stirring for half hour. n temperature was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl 0.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was on stirring for 24 h, and color of the mixture changed from yellow to dark orange. us mixture was poured into ice water. Precipitates were collected by filtration and then deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and in deionized water. After filtration, it was washed with Ethanol (500 mL × 3). Tosylated btained was dried below 50 °C in oven.  [27].
itution of CTOS with Amines to Synthesize 6-Deoxy-Aminocellulose es of cellulose amine derivatives were produced by substitution of tosyl group. Tosylated TOS) (2 g) was dissolved in 2 ml of DMF with constant stirring. A total of 25 equivalents er Hydrazinium hydroxide, Diethylamine or Diethylenetriamine per AGU in 10 mL of g 1 ml of TEA were drop wise added to viscous solution of CTOS with constant stirring at tion was continuously refluxed at 90 °C for 24 h while progress was monitored by TLC. ixture was dialyzed in deionized water and ethanol to obtain the product. Obtained lymeric product was collected by filtration and dried at 50 °C under vacuum. y-6-hydrazide Cellulose (Cell-Hyd) Tea pink powder = 1.69 g, yield 84%, Elemental age Found), C = 41. 34

Tosylation of Cellulose
Dried microcrystalline Cellulose MCC, 10 g (61.6 mM of anhydrous glucose unit (AGU)) was taken in 1000 mL flask, and 250 mL of N,N-Dimethyl acetamide synthetic grade (DMA) was added and stirred at 120 °C for 1 h. Resulting slurry was cooled to 100 °C, and then, Lithium Chloride Anhydrous LiCl, (20 g) in DMA (50 mL), was added dropwise. Stirring was continued overnight until the complete dissolution of the Cellulose. A volume of 37.2 mL of Triethylamine (TEA) (370 mM), 6 mol/AGU in 20 mL of DMA, was added to the cellulose solution at constant stirring for half hour. The solution temperature was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl chloride (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was continued on stirring for 24 h, and color of the mixture changed from yellow to dark orange. Homogenous mixture was poured into ice water. Precipitates were collected by filtration and then washed by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and recollected in deionized water. After filtration, it was washed with Ethanol (500 mL × 3). Tosylated Cellulose obtained was dried below 50 °C in oven. Tosylated

2.2.2.
Subsitution of CTOS with Amines to Synthesize 6-Deoxy-Aminocellulose A series of cellulose amine derivatives were produced by substitution of tosyl group. Tosylated cellulose (CTOS) (2 g) was dissolved in 2 ml of DMF with constant stirring. A total of 25 equivalents [28] of either Hydrazinium hydroxide, Diethylamine or Diethylenetriamine per AGU in 10 mL of DMF having 1 ml of TEA were drop wise added to viscous solution of CTOS with constant stirring at 90 °C. Reaction was continuously refluxed at 90 °C for 24 h while progress was monitored by TLC. Reaction mixture was dialyzed in deionized water and ethanol to obtain the product. Obtained derived polymeric product was collected by filtration and dried at 50 °C under vacuum.

Tosylation of Cellulose
Dried microcrystalline Cellulose MCC, 10 g (61.6 mM of anhydrous glucose unit (AGU)) was taken in 1000 mL flask, and 250 mL of N,N-Dimethyl acetamide synthetic grade (DMA) was added and stirred at 120 °C for 1 h. Resulting slurry was cooled to 100 °C, and then, Lithium Chloride Anhydrous LiCl, (20 g) in DMA (50 mL), was added dropwise. Stirring was continued overnight until the complete dissolution of the Cellulose. A volume of 37.2 mL of Triethylamine (TEA) (370 mM), 6 mol/AGU in 20 mL of DMA, was added to the cellulose solution at constant stirring for half hour. The solution temperature was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl chloride (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was continued on stirring for 24 h, and color of the mixture changed from yellow to dark orange. Homogenous mixture was poured into ice water. Precipitates were collected by filtration and then washed by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and recollected in deionized water. After filtration, it was washed with Ethanol (500 mL × 3). Tosylated Cellulose obtained was dried below 50 °C in oven. Tosylated

2.2.2.
Subsitution of CTOS with Amines to Synthesize 6-Deoxy-Aminocellulose A series of cellulose amine derivatives were produced by substitution of tosyl group. Tosylated cellulose (CTOS) (2 g) was dissolved in 2 ml of DMF with constant stirring. A total of 25 equivalents [28] of either Hydrazinium hydroxide, Diethylamine or Diethylenetriamine per AGU in 10 mL of DMF having 1 ml of TEA were drop wise added to viscous solution of CTOS with constant stirring at 90 °C. Reaction was continuously refluxed at 90 °C for 24 h while progress was monitored by TLC. Reaction mixture was dialyzed in deionized water and ethanol to obtain the product. Obtained derived polymeric product was collected by filtration and dried at 50 °C under vacuum.

Tosylation of Cellulose
Dried microcrystalline Cellulose MCC, 10 g (61.6 mM of anhydrous glucose unit (AGU)) taken in 1000 mL flask, and 250 mL of N,N-Dimethyl acetamide synthetic grade (DMA) was ad and stirred at 120 °C for 1 h. Resulting slurry was cooled to 100 °C, and then, Lithium Chlor Anhydrous LiCl, (20 g) in DMA (50 mL), was added dropwise. Stirring was continued overnight u the complete dissolution of the Cellulose. A volume of 37.2 mL of Triethylamine (TEA) (370 mM mol/AGU in 20 mL of DMA, was added to the cellulose solution at constant stirring for half ho The solution temperature was dropped from room temperature to 3-8 °C, and p-Toluene sulfo chloride (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction continued on stirring for 24 h, and color of the mixture changed from yellow to dark oran Homogenous mixture was poured into ice water. Precipitates were collected by filtration and t washed by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone recollected in deionized water. After filtration, it was washed with Ethanol (500 mL × 3). Tosyla Cellulose obtained was dried below 50 °C in oven.

Tosylation of Cellulose
Dried microcrystalline Cellulose MCC, 10 g (61.6 mM of anhydrous g taken in 1000 mL flask, and 250 mL of N,N-Dimethyl acetamide synthetic g and stirred at 120 °C for 1 h. Resulting slurry was cooled to 100 °C, and Anhydrous LiCl, (20 g) in DMA (50 mL), was added dropwise. Stirring was c the complete dissolution of the Cellulose. A volume of 37.2 mL of Triethyla mol/AGU in 20 mL of DMA, was added to the cellulose solution at consta The solution temperature was dropped from room temperature to 3-8 °C chloride (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was add continued on stirring for 24 h, and color of the mixture changed from Homogenous mixture was poured into ice water. Precipitates were collect washed by deionized water (8 L) and 1 L of ethanol, suspended in 500 m recollected in deionized water. After filtration, it was washed with Ethano Cellulose obtained was dried below 50 °C in oven. Cellulose MCC, 10 g (61.6 mM of anhydrous glucose unit (AGU)) was 1000 mL flask, and 250 mL of N,N-Dimethyl acetamide synthetic grade (DMA) was added rred at 120 °C for 1 h. Resulting slurry was cooled to 100 °C, and then, Lithium Chloride rous LiCl, (20 g) in DMA (50 mL), was added dropwise. Stirring was continued overnight until plete dissolution of the Cellulose. A volume of 37.2 mL of Triethylamine (TEA) (370 mM), 6 U in 20 mL of DMA, was added to the cellulose solution at constant stirring for half hour. ution temperature was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl e (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was ed on stirring for 24 h, and color of the mixture changed from yellow to dark orange. enous mixture was poured into ice water. Precipitates were collected by filtration and then by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and ted in deionized water. After filtration, it was washed with Ethanol (500 mL × 3 A series of cellulose amine derivatives were produced by substitution of tosyl group. Tosylated cellulose (C TOS ) (2 g) was dissolved in 2 ml of DMF with constant stirring. A total of 25 equivalents [28] of either Hydrazinium hydroxide, Diethylamine or Diethylenetriamine per AGU in 10 mL of DMF having 1 ml of TEA were drop wise added to viscous solution of C TOS with constant stirring at 90 • C. Reaction was continuously refluxed at 90 • C for 24 h while progress was monitored by TLC. Reaction mixture was dialyzed in deionized water and ethanol to obtain the product. Obtained derived polymeric product was collected by filtration and dried at 50 • C under vacuum.
6-deoxy-6-hydrazide Cellulose (Cell-Hyd) Tea pink powder = 1.69 g, yield 84%, Elemental Analysis (%age Found), C = 41.34, H = 6.64, N = 7.95. FTIR cm −1 : 3294, 3330 (broad mol/AGU in 20 mL of DMA, was added to the cellulose solution at con The solution temperature was dropped from room temperature to 3-8 chloride (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was a continued on stirring for 24 h, and color of the mixture changed fro Homogenous mixture was poured into ice water. Precipitates were coll washed by deionized water (8 L) and 1 L of ethanol, suspended in 500 recollected in deionized water. After filtration, it was washed with Etha Cellulose obtained was dried below 50 °C in oven. olution of the Cellulose. A volume of 37.2 mL of Triethylamine (TEA) (370 mM), 6 L of DMA, was added to the cellulose solution at constant stirring for half hour. perature was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl 69.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was ring for 24 h, and color of the mixture changed from yellow to dark orange. ture was poured into ice water. Precipitates were collected by filtration and then ized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and onized water. After filtration, it was washed with Ethanol (500 mL × 3). Tosylated d was dried below 50 °C in oven. llulose (CTOS): White powder = 7.03 g, yield 77%, Elemental Analysis (%age Found); 4, S = 5.01, DS (Degree of Tosylation) = 0.48 (based on sulfur analysis), FTIR cm −1 : 7 (ⱱCH), 1619 (ⱱasym ⱱ , 1358 (ⱱassymSO2), 1172 (ⱱsymSO2), 812 (ⱱaromC-H) 1358, DMSO-d6) δ ppm: 7.75 (d, 2H, ortho), 7.35 (d, 2H, para), 4.94-3.99 (m, 1H, CH), CH), 3.14-3.00 (m, 1H, CH), 2.42 (s, 3H, tosyl CH3). 13  AGU in 20 mL of DMA, was added to the cellulose solution at constant stirring for half hour. solution temperature was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl ide (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was nued on stirring for 24 h, and color of the mixture changed from yellow to dark orange. ogenous mixture was poured into ice water. Precipitates were collected by filtration and then ed by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and lected in deionized water. After filtration, it was washed with Ethanol (500 mL × 3). Tosylated lose obtained was dried below 50 °C in oven.  The solution temperature was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl chloride (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was continued on stirring for 24 h, and color of the mixture changed from yellow to dark orange. Homogenous mixture was poured into ice water. Precipitates were collected by filtration and then washed by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and recollected in deionized water. After filtration, it was washed with Ethanol (500 mL × 3). Tosylated Cellulose obtained was dried below 50 °C in oven. the complete dissolution of the Cellulose. A volume of 37.2 mL of Triethylamine (TEA) (370 mM), 6 mol/AGU in 20 mL of DMA, was added to the cellulose solution at constant stirring for half hour. The solution temperature was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl chloride (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was continued on stirring for 24 h, and color of the mixture changed from yellow to dark orange. Homogenous mixture was poured into ice water. Precipitates were collected by filtration and then washed by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and recollected in deionized water. After filtration, it was washed with Ethanol (500 mL × 3). Tosylated Cellulose obtained was dried below 50 °C in oven. (20 g) in DMA (50 mL), was added dropwise. Stirring was continued overnight until olution of the Cellulose. A volume of 37.2 mL of Triethylamine (TEA) (370 mM), 6 L of DMA, was added to the cellulose solution at constant stirring for half hour. perature was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl 69.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was rring for 24 h, and color of the mixture changed from yellow to dark orange. ture was poured into ice water. Precipitates were collected by filtration and then ized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and onized water. After filtration, it was washed with Ethanol (500 mL × 3). Tosylated d was dried below 50 °C in oven. llulose (CTOS): White powder = 7.03 g, yield 77%, Elemental Analysis (%age Found); 4, S = 5.01, DS (Degree of Tosylation) = 0.48 (based on sulfur analysis), FTIR cm −1 : 7 (ⱱCH), 1619 (ⱱasym ⱱ , 1358 (ⱱassymSO2), 1172 (ⱱsymSO2), 812 (ⱱaromC-H) 1358, DMSO-d6) δ ppm: 7.75 (d, 2H, ortho), 7.35 (d, 2H, para), 4.94-3.99 (m, 1H, CH), CH), 3.14-3.00 (m, 1H, CH), 2.42 (s, 3H, tosyl CH3). 13 C Cellulose MCC, 10 g (61.6 mM of anhydrous glu taken in 1000 mL flask, and 250 mL of N,N-Dimethyl acetamide synthetic gra and stirred at 120 °C for 1 h. Resulting slurry was cooled to 100 °C, and th Anhydrous LiCl, (20 g) in DMA (50 mL), was added dropwise. Stirring was con the complete dissolution of the Cellulose. A volume of 37.2 mL of Triethylami mol/AGU in 20 mL of DMA, was added to the cellulose solution at constant The solution temperature was dropped from room temperature to 3-8 °C, an chloride (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added continued on stirring for 24 h, and color of the mixture changed from ye Homogenous mixture was poured into ice water. Precipitates were collected washed by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL o recollected in deionized water. After filtration, it was washed with Ethanol (5 Cellulose obtained was dried below 50 °C in oven. Tosylated

Subsitution of CTOS with Amines to Synthesize 6-Deoxy-Aminocellulose
A series of cellulose amine derivatives were produced by substitution of t cellulose (CTOS) (2 g) was dissolved in 2 ml of DMF with constant stirring. A t [28] of either Hydrazinium hydroxide, Diethylamine or Diethylenetriamine DMF having 1 ml of TEA were drop wise added to viscous solution of CTOS w 90 °C. Reaction was continuously refluxed at 90 °C for 24 h while progress w Reaction mixture was dialyzed in deionized water and ethanol to obtain t derived polymeric product was collected by filtration and dried at 50 °C unde 6-deoxy-6-hydrazide Cellulose (Cell-Hyd) Tea pink powder = 1. lulose lline Cellulose MCC, 10 g (61.6 mM of anhydrous glucose unit (AGU)) was , and 250 mL of N,N-Dimethyl acetamide synthetic grade (DMA) was added for 1 h. Resulting slurry was cooled to 100 °C, and then, Lithium Chloride in DMA (50 mL), was added dropwise. Stirring was continued overnight until n of the Cellulose. A volume of 37.2 mL of Triethylamine (TEA) (370 mM), 6 DMA, was added to the cellulose solution at constant stirring for half hour. ure was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl M, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was for 24 h, and color of the mixture changed from yellow to dark orange. was poured into ice water. Precipitates were collected by filtration and then water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and d water. After filtration, it was washed with Ethanol (500 mL × 3). Tosylated dried below 50 °C in oven. 6 mM of anhydrous glucose unit (AGU)) was 1000 mL flask, and 250 mL of N,N-Dimethyl acetamide synthetic grade (DMA) was added ed at 120 °C for 1 h. Resulting slurry was cooled to 100 °C, and then, Lithium Chloride us LiCl, (20 g) in DMA (50 mL), was added dropwise. Stirring was continued overnight until lete dissolution of the Cellulose. A volume of 37.2 mL of Triethylamine (TEA) (370 mM), 6 in 20 mL of DMA, was added to the cellulose solution at constant stirring for half hour. tion temperature was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was d on stirring for 24 h, and color of the mixture changed from yellow to dark orange. nous mixture was poured into ice water. Precipitates were collected by filtration and then by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and ed in deionized water. After filtration, it was washed with Ethanol (500 mL × 3). Tosylated obtained was dried below 50 °C in oven.

Tosylation of Cellulose
Dried microcrystalline Cellulose MCC, 10 g (61.6 mM of anhydrous glucose unit (AGU)) was taken in 1000 mL flask, and 250 mL of N,N-Dimethyl acetamide synthetic grade (DMA) was added and stirred at 120 °C for 1 h. Resulting slurry was cooled to 100 °C, and then, Lithium Chloride Anhydrous LiCl, (20 g) in DMA (50 mL), was added dropwise. Stirring was continued overnight until the complete dissolution of the Cellulose. A volume of 37.2 mL of Triethylamine (TEA) (370 mM), 6 mol/AGU in 20 mL of DMA, was added to the cellulose solution at constant stirring for half hour. The solution temperature was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl chloride (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was continued on stirring for 24 h, and color of the mixture changed from yellow to dark orange. Homogenous mixture was poured into ice water. Precipitates were collected by filtration and then washed by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and recollected in deionized water. After filtration, it was washed with Ethanol (500 mL × 3). Tosylated Cellulose obtained was dried below 50 °C in oven.
Tosylated Dried microcrystalline Cellulose MCC, 10 g (61.6 mM of anhydrous glucose unit (AGU taken in 1000 mL flask, and 250 mL of N,N-Dimethyl acetamide synthetic grade (DMA) was and stirred at 120 °C for 1 h. Resulting slurry was cooled to 100 °C, and then, Lithium C Anhydrous LiCl, (20 g) in DMA (50 mL), was added dropwise. Stirring was continued overnig the complete dissolution of the Cellulose. A volume of 37.2 mL of Triethylamine (TEA) (370 mol/AGU in 20 mL of DMA, was added to the cellulose solution at constant stirring for ha The solution temperature was dropped from room temperature to 3-8 °C, and p-Toluene s chloride (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reacti continued on stirring for 24 h, and color of the mixture changed from yellow to dark Homogenous mixture was poured into ice water. Precipitates were collected by filtration an washed by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling aceto recollected in deionized water. After filtration, it was washed with Ethanol (500 mL × 3). To Cellulose obtained was dried below 50 °C in oven.

Tosylation of Cellulose
Dried microcrystalline Cellulose MCC, 10 g (61.6 mM of anhydrous taken in 1000 mL flask, and 250 mL of N,N-Dimethyl acetamide synthetic and stirred at 120 °C for 1 h. Resulting slurry was cooled to 100 °C, an Anhydrous LiCl, (20 g) in DMA (50 mL), was added dropwise. Stirring was the complete dissolution of the Cellulose. A volume of 37.2 mL of Triethy mol/AGU in 20 mL of DMA, was added to the cellulose solution at cons The solution temperature was dropped from room temperature to 3-8 °C chloride (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was ad continued on stirring for 24 h, and color of the mixture changed from Homogenous mixture was poured into ice water. Precipitates were collec washed by deionized water (8 L) and 1 L of ethanol, suspended in 500 m recollected in deionized water. After filtration, it was washed with Ethan Cellulose obtained was dried below 50 °C in oven. cation. Dulbecco's Modified Eagle Medium (DMEM), TrypLE Express Enzyme (1×), Penicillintomycin (10,000 U/mL) Fetal Bovine Serum (FBS) and phosphate buffered saline (PBS) were ed from (Gibco, Thermo Fisher Scientific Inc., Waltham, MA, USA). NIH3T3, B16F10, MDA-31 and MCF-7 cell lines were obtained from American Type Culture Collection (ATCC), assas, VA, USA).

ethod
Tosylation of Cellulose ried microcrystalline Cellulose MCC, 10 g (61.6 mM of anhydrous glucose unit (AGU)) was in 1000 mL flask, and 250 mL of N,N-Dimethyl acetamide synthetic grade (DMA) was added tirred at 120 °C for 1 h. Resulting slurry was cooled to 100 °C, and then, Lithium Chloride drous LiCl, (20 g) in DMA (50 mL), was added dropwise. Stirring was continued overnight until mplete dissolution of the Cellulose. A volume of 37.2 mL of Triethylamine (TEA) (370 mM), 6 GU in 20 mL of DMA, was added to the cellulose solution at constant stirring for half hour. olution temperature was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl de (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was ued on stirring for 24 h, and color of the mixture changed from yellow to dark orange. genous mixture was poured into ice water. Precipitates were collected by filtration and then ed by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and ected in deionized water. After filtration, it was washed with Ethanol (500 mL × 3). Tosylated lose obtained was dried below 50 °C in oven.  [27].

Subsitution of CTOS
with Amines to Synthesize 6-Deoxy-Aminocellulose series of cellulose amine derivatives were produced by substitution of tosyl group. Tosylated ose (CTOS) (2 g) was dissolved in 2 ml of DMF with constant stirring. A total of 25 equivalents f either Hydrazinium hydroxide, Diethylamine or Diethylenetriamine per AGU in 10 mL of having 1 ml of TEA were drop wise added to viscous solution of CTOS with constant stirring at . Reaction was continuously refluxed at 90 °C for 24 h while progress was monitored by TLC. ion mixture was dialyzed in deionized water and ethanol to obtain the product. Obtained ed polymeric product was collected by filtration and dried at 50 °C under vacuum.

Tosylation of Cellulose
Dried microcrystalline Cellulose MCC, 10 g (61.6 mM of anhydrous glucose unit (AGU)) was taken in 1000 mL flask, and 250 mL of N,N-Dimethyl acetamide synthetic grade (DMA) was added and stirred at 120 °C for 1 h. Resulting slurry was cooled to 100 °C, and then, Lithium Chloride Anhydrous LiCl, (20 g) in DMA (50 mL), was added dropwise. Stirring was continued overnight until the complete dissolution of the Cellulose. A volume of 37.2 mL of Triethylamine (TEA) (370 mM), 6 mol/AGU in 20 mL of DMA, was added to the cellulose solution at constant stirring for half hour. The solution temperature was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl chloride (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was continued on stirring for 24 h, and color of the mixture changed from yellow to dark orange. Homogenous mixture was poured into ice water. Precipitates were collected by filtration and then washed by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and recollected in deionized water. After filtration, it was washed with Ethanol (500 mL × 3

2.2.2.
Subsitution of CTOS with Amines to Synthesize 6-Deoxy-Aminocellulose A series of cellulose amine derivatives were produced by substitution of tosyl group. Tosylated cellulose (CTOS) (2 g) was dissolved in 2 ml of DMF with constant stirring. A total of 25 equivalents [28] of either Hydrazinium hydroxide, Diethylamine or Diethylenetriamine per AGU in 10 mL of DMF having 1 ml of TEA were drop wise added to viscous solution of CTOS with constant stirring at 90 °C. Reaction was continuously refluxed at 90 °C for 24 h while progress was monitored by TLC. Reaction mixture was dialyzed in deionized water and ethanol to obtain the product. Obtained derived polymeric product was collected by filtration and dried at 50 °C under vacuum.

Tosylation of Cellulose
Dried microcrystalline Cellulose MCC, 10 g (61.6 mM of anhydrous glucose unit (AGU)) was taken in 1000 mL flask, and 250 mL of N,N-Dimethyl acetamide synthetic grade (DMA) was added and stirred at 120 °C for 1 h. Resulting slurry was cooled to 100 °C, and then, Lithium Chloride Anhydrous LiCl, (20 g) in DMA (50 mL), was added dropwise. Stirring was continued overnight until the complete dissolution of the Cellulose. A volume of 37.2 mL of Triethylamine (TEA) (370 mM), 6 mol/AGU in 20 mL of DMA, was added to the cellulose solution at constant stirring for half hour. The solution temperature was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl chloride (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was continued on stirring for 24 h, and color of the mixture changed from yellow to dark orange. Homogenous mixture was poured into ice water. Precipitates were collected by filtration and then washed by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and recollected in deionized water. After filtration, it was washed with Ethanol (500 mL × 3). Tosylated Cellulose obtained was dried below 50 °C in oven. Tosylated

Tosylation of Cellulose
Dried microcrystalline Cellulose MCC, 10 g (61.6 mM of anhydrous glucose unit (AGU)) was taken in 1000 mL flask, and 250 mL of N,N-Dimethyl acetamide synthetic grade (DMA) was added and stirred at 120 °C for 1 h. Resulting slurry was cooled to 100 °C, and then, Lithium Chloride Anhydrous LiCl, (20 g) in DMA (50 mL

2.2.2.
Subsitution of CTOS with Amines to Synthesize 6-Deoxy-Aminocellulose A series of cellulose amine derivatives were produced by substitution of tosyl group. Tosylated cellulose (CTOS) (2 g) was dissolved in 2 ml of DMF with constant stirring. A total of 25 equivalents [28] of either Hydrazinium hydroxide, Diethylamine or Diethylenetriamine per AGU in 10 mL of DMF having 1 ml of TEA were drop wise added to viscous solution of CTOS with constant stirring at 90 °C. Reaction was continuously refluxed at 90 °C for 24 h while progress was monitored by TLC. Reaction mixture was dialyzed in deionized water and ethanol to obtain the product. Obtained derived polymeric product was collected by filtration and dried at 50 °C under vacuum.

Measurement
FTIR spectra were recorded on Bruker attenuated total reflectance Fourier transform infrared (ATR FT-IR) spectrophotometer (Bruker platinum ATR model Alpha spectrophotometer, Karlsruhe, Germany). Twenty mg of samples was scanned over 4000 to 400 cm −1 wave number. 1 HNMR spectra were recorded for all samples at room temperature in deuterated dimethyl sulfoxide (DMSO-d6) on a 400 MHz Bruker AV400 spectrometer (Bruker Corporation, Billerica, MA, USA) with 64 scans for concentration of 20 mg/mL −1 . SEM Morphological studies of the powdered derivatives were checked on SEM (JSM-64900) with (EDX) spectrometer (JEOL, Akishima, Japan). Samples were sputter coated with iridium using South Bay Technology Ion Beam Sputtering/Etching System. After sputter coating, sample morphology was observed under SEM Elemental analyses were carried out on a CKIC 5E-CHNS-2200 and CKIC5E-IRS II ultimate analyzer (CHANGSHA KAIYUAN INSTRUMENTS CO LTD., Changsha, China). X-ray Diffraction patterns of cellulose and its derivatives were recorded with a X-ray diffractometer (D8 advance BRUKER, Billerica, MA, USA) in transmission mode over 2θ ranges 5−80 • with Cu Kα radiation. Phase conformation of the synthesized nanomaterials was also confirmed at 40 kV voltage and 40 mA current while the instrument uses Cu Ka radiation (λ = 1.54060 Å) for X-ray production. Zeta potential ζ Zeta potential was measured on a Zetasizer NanoS Series (Malvern Panalytical Ltd., Worcestershire, UK). Samples 1 mg/10 mL in deionized water were suspended using a sonication bath for half an hour before testing in a disposable folded capillary cell at 37 • C. Furthermore, the samples were incubated at 37 • C for 48 h under constant stirring before recording the zeta potential measurements to check the stability of zeta potential. The ζpotential plot was analyzed using the Zetasizer software PCS V.1.4 (Malvern Instruments, Malvern, UK). Swelling ratios of the samples were determined by taking 10 mg sample in pre weighed Eppendorf tubes with 1 ml of Dulbecco's phosphate-buffered saline (DPBS). After 24 h, DPBS was removed from samples, and samples were again weighed. Swelling ratios were calculated by following formula (weight of the wet sample/weight of dry sample × 100). Cell culture In vitro cytotoxicity of the synthesized cellulose derivatives was evaluated against 4 cell lines. One fibroblast cell line NIH3T3 (mouse embryo fibroblasts) and three cancer cell lines B16F10 (mouse skin melanoma), MDA-MB-231(human epithelial adenocarcinoma) and MCF-7 (human breast adenocarcinoma) were used to calculate the IC 50 values. Frozen Cell lines were passaged in DMEM supplemented with 10% FBS and 1% Penstrep five times at 37 • C and humidified air with 5% CO 2 . Cell viability and cytotoxicity index IC 50 values were determined by seeding the 96 well plates at concentration 30,000 cells/mL or 10,000 cells/cm 2 for each cell line and incubating at 37 • C in humidified air with 5% CO 2 . After 24 h, media was removed, and cells were washed with PBS to remove any dead cells. Then, 100 ul of serial diluted concentrations of cellulose and its derivatives (5, 10, 20, 40, 60, 80, 100, 150, 200, 250, 500 and 1000 µg/mL) was added to each well and incubated in the same condition for the next 24 h. Cellulose and its derivatives were dissolved in DMSO (maximum concentration of DMSO in the 0.5% per well) and then diluted in DMEM. Untreated cell wells were only media added to serve as control and were incubated for 24 h. Media was removed after 24 h, and cells were incubated for 2 h with PrestoBlue Cell viability Reagent (10% PrestoBlue in DMEM). Cell viability and cytotoxicity index IC 50 was calculated by reading the plate on a plate reader at fluorescence intensity excitation/emission 535-560/590-615. Triplicate samples were used for analysis. Prism-GraphPad-5 was used to draw the IC 50 Curves with standard errors, and then, IC 50 values were calculated. All data were presented here as an average ± standard deviation (S.D.), and p < 0.05 considered as significant difference. All cell experiments were performed with triplicate samples in 3 independent experiments. Prism-GraphPad 5 was used to analyze the results and create figures. Nonlinear regression curve fit (Dose-response) was used to plot the cytotoxicity results of each compounds thereby. IC 50 values were obtained. The obtained IC 50 values were subjected to one-way ANOVA analysis using an appropriate Tukey to compare all pairs of columns test for statistical comparison. In figures, statistical significance was defined as * p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001. Live/Dead Assay was carried out at 24h stage according to the protocol for LIVE/DEAD ® Viability/Cytotoxicity Kit (mammalian cells). Cells were cultured according to same protocol as above at IC 50 value for 24 h. Untreated cells were used as control. Cells were washed with PBS and then Calcein AM (1 µL/mL of 50 µM stock) Ethidium homodimer-1 (2 µL/mL of the 2 mM stock) 50 ul was added to each well. Plate was incubated for 30 to 40 min, and then, the cells were observed on inverted fluorescence microscope (Zeiss Axio Observer Z1, Zeiss, Germany) at 494/517 nm for Calcein-AM (live cells as green indicating intracellular esterate activity) and at 528/617 nm ethidium homodimer (dead cells as red indicate loss of plasma membrane activity). Number of live cells were counted by Image J (US National Institutes of Health, Bethesda, MD, USA) software and from four random fields of 3 replicates of samples. Live cell percentage was counted by dividing number of live cells by total number of cells. Four random field images were taken at 10×.

Tosylation
Tosylated Cellulose (C TOS ) with degree of substitution (DS) 0.48 was obtained by previously reported method Rahn et al. [29]. Shortly, Cellulose was reacted with 6 equivalent of tosyl chloride by dissolving Cellulose in N,N-dimethylacetamide/LiCl with 6 equivalent Triethylamine for 24 h at 10°C. Lower temperature and Triethylamine [30] minimize the formation of 6-deoxy-6-chloro groups [31]. It has been reported that tosylation reaction occurs preferably at position 6 rather than positions 2 and 3 [29]. A total of 6 equivalents of p-tosyl chloride against hydroxyl group increases the DS from 0.3 to 0.5 with percentage yield corresponding to 77%. Lab synthesized Tosylated cellulose (C TOS ) was evaluated by FTIR, NMR and Elemental analysis (for degree of substitution). Infrared spectroscopy cannot fully explicate the structure but gives useful information about the functional group. Cellulose MCC, 10 g (61.6 mM of anhydrous glucose unit (AGU)) was 1000 mL flask, and 250 mL of N,N-Dimethyl acetamide synthetic grade (DMA) was added red at 120 °C for 1 h. Resulting slurry was cooled to 100 °C, and then, Lithium Chloride ous LiCl, (20 g) in DMA (50 mL), was added dropwise. Stirring was continued overnight until plete dissolution of the Cellulose. A volume of 37.2 mL of Triethylamine (TEA) (370 mM), 6 U in 20 mL of DMA, was added to the cellulose solution at constant stirring for half hour. ution temperature was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl e (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was ed on stirring for 24 h, and color of the mixture changed from yellow to dark orange. enous mixture was poured into ice water. Precipitates were collected by filtration and then by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and ted in deionized water. After filtration, it was washed with Ethanol (500 mL × 3). Tosylated se obtained was dried below 50 °C in oven.

Materials
All chemicals and reagents, viz.

Tosylation of Cellulose
Dried microcrystalline Cellulose MCC, 10 g (61.6 mM of anhydrous glucose unit (AGU)) was taken in 1000 mL flask, and 250 mL of N,N-Dimethyl acetamide synthetic grade (DMA) was added and stirred at 120 °C for 1 h. Resulting slurry was cooled to 100 °C, and then, Lithium Chloride Anhydrous LiCl, (20 g) in DMA (50 mL), was added dropwise. Stirring was continued overnight until the complete dissolution of the Cellulose. A volume of 37.2 mL of Triethylamine (TEA) (370 mM), 6 mol/AGU in 20 mL of DMA, was added to the cellulose solution at constant stirring for half hour. The solution temperature was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl chloride (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was continued on stirring for 24 h, and color of the mixture changed from yellow to dark orange. Homogenous mixture was poured into ice water. Precipitates were collected by filtration and then washed by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and recollected in deionized water. After filtration, it was washed with Ethanol (500 mL × 3). Tosylated Cellulose obtained was dried below 50 °C in oven. Tosylated

Materials
All chemicals and reagents, viz.

Tosylation of Cellulose
Dried microcrystalline Cellulose MCC, 10 g (61.6 mM of anhydrous gluc taken in 1000 mL flask, and 250 mL of N,N-Dimethyl acetamide synthetic grad and stirred at 120 °C for 1 h. Resulting slurry was cooled to 100 °C, and the Anhydrous LiCl, (20 g) in DMA (50 mL), was added dropwise. Stirring was cont the complete dissolution of the Cellulose. A volume of 37.2 mL of Triethylamin mol/AGU in 20 mL of DMA, was added to the cellulose solution at constant s The solution temperature was dropped from room temperature to 3-8 °C, an chloride (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added continued on stirring for 24 h, and color of the mixture changed from yel Homogenous mixture was poured into ice water. Precipitates were collected b washed by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of recollected in deionized water. After filtration, it was washed with Ethanol (

Materials
All chemicals and reagents, viz., Cellulose, microcrystalline

Tosylation of Cellulose
Dried microcrystalline Cellulose MCC, 10 g (61.6 mM of a taken in 1000 mL flask, and 250 mL of N,N-Dimethyl acetamide and stirred at 120 °C for 1 h. Resulting slurry was cooled to 1 Anhydrous LiCl, (20 g)   The solution temperature was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl chloride (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was continued on stirring for 24 h, and color of the mixture changed from yellow to dark orange. Homogenous mixture was poured into ice water. Precipitates were collected by filtration and then washed by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and recollected in deionized water. After filtration, it was washed with Ethanol (500 mL × 3  18 (m, 5H, CH), 3.14-3.00 (m, 1H, CH), 2.42 (s, 3H, tosyl CH3). 13  The solution temperature was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl chloride (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was continued on stirring for 24 h, and color of the mixture changed from yellow to dark orange. Homogenous mixture was poured into ice water. Precipitates were collected by filtration and then washed by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and recollected in deionized water. After filtration, it was washed with Ethanol (500 mL × 3  18 (m, 5H, CH), 3.14-3.00 (m, 1H, CH), 2.42 (s, 3H, tosyl CH3). 13  The solution temperature was dropped from room temperature to 3-8 °C, and p-Toluene chloride (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Rea continued on stirring for 24 h, and color of the mixture changed from yellow to dar Homogenous mixture was poured into ice water. Precipitates were collected by filtration washed by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling ace recollected in deionized water. After filtration, it was washed with Ethanol (500 mL × 3  18 (m, 5H, CH), 3.14-3.00 (m, 1H, CH), 2.42 (s, 3H, tosyl CH3). 13

Subsitution of CTOS with Amines to Synthesize 6-Deoxy-Aminocellulose
A series of cellulose amine derivatives were produced by substitution of tosyl group. cellulose (CTOS) (2 g) was dissolved in 2 ml of DMF with constant stirring. A total of 25 eq [28] of either Hydrazinium hydroxide, Diethylamine or Diethylenetriamine per AGU in DMF having 1 ml of TEA were drop wise added to viscous solution of CTOS with constant 90 °C. Reaction was continuously refluxed at 90 °C for 24 h while progress was monitored Reaction mixture was dialyzed in deionized water and ethanol to obtain the product. derived polymeric product was collected by filtration and dried at 50 °C under vacuum.
6-deoxy-6-hydrazide Cellulose (Cell-Hyd) Tea pink powder = 1.69 g, yield 84%, E Analysis (%age Found), C = 41.34, H = 6.64, N = 7.95. FTIR cm −1 : 3294, 3330 (broad ⱱstrN-H,-arom C-H), along with tosyl SO 2 group appeared at 1358 ( mol/AGU in 20 mL of DMA, was added to the cellulose solution at constant stirring for half hour. The solution temperature was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl chloride (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was continued on stirring for 24 h, and color of the mixture changed from yellow to dark orange. Homogenous mixture was poured into ice water. Precipitates were collected by filtration and then washed by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and recollected in deionized water. After filtration, it was washed with Ethanol (500 mL × 3). Tosylated Cellulose obtained was dried below 50 °C in oven. Tosylated

Subsitution of CTOS with Amines to Synthesize 6-Deoxy-Aminocellulose
A series of cellulose amine derivatives were produced by substitution of tosyl group. Tosylated cellulose (CTOS) (2 g) was dissolved in 2 ml of DMF with constant stirring. A total of 25 equivalents [28] of either Hydrazinium hydroxide, Diethylamine or Diethylenetriamine per AGU in 10 mL of DMF having 1 ml of TEA were drop wise added to viscous solution of CTOS with constant stirring at 90 °C. Reaction was continuously refluxed at 90 °C for 24 h while progress was monitored by TLC. Reaction mixture was dialyzed in deionized water and ethanol to obtain the product. Obtained derived polymeric product was collected by filtration and dried at 50 °C under vacuum.
6-deoxy-6-hydrazide Cellulose (Cell-Hyd) Tea pink powder = 1.69 g, yield 84%, Elemental Analysis (%age Found), C = 41.34, H = 6.64, N = 7.95. FTIR cm −1 : 3294, 3330 (broad ⱱstrN-H,-OH) 2889 assym SO 2 ), 1172 ( mol/AGU in 20 mL of DMA, was added to the cellulose solution at constant stirring for half hour. The solution temperature was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl chloride (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was continued on stirring for 24 h, and color of the mixture changed from yellow to dark orange. Homogenous mixture was poured into ice water. Precipitates were collected by filtration and then washed by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and recollected in deionized water. After filtration, it was washed with Ethanol (500 mL × 3). Tosylated Cellulose obtained was dried below 50 °C in oven.
Tosylated mol/AGU in 20 mL of DMA, was added to the cellulose solution at constant stirring for half hour. The solution temperature was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl chloride (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was continued on stirring for 24 h, and color of the mixture changed from yellow to dark orange. Homogenous mixture was poured into ice water. Precipitates were collected by filtration and then washed by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and recollected in deionized water. After filtration, it was washed with Ethanol (500 mL × 3). Tosylated Cellulose obtained was dried below 50 °C in oven. Tosylated

Subsitution of CTOS with Amines to Synthesize 6-Deoxy-Aminocellulose
A series of cellulose amine derivatives were produced by substitution of tosyl group. Tosylated cellulose (CTOS) (2 g) was dissolved in 2 ml of DMF with constant stirring. A total of 25 equivalents [28] of either Hydrazinium hydroxide, Diethylamine or Diethylenetriamine per AGU in 10 mL of DMF having 1 ml of TEA were drop wise added to viscous solution of CTOS with constant stirring at 90 °C. Reaction was continuously refluxed at 90 °C for 24 h while progress was monitored by TLC. Reaction mixture was dialyzed in deionized water and ethanol to obtain the product. Obtained derived polymeric product was collected by filtration and dried at 50 °C under vacuum.
6-deoxy-6-hydrazide Cellulose (Cell-Hyd) Tea pink powder = 1.69 g, yield 84%, Elemental Analysis (%age Found), C = 41.34, H = 6.64, N = 7.95. FTIR cm −1 : 3294, 3330 (broad ⱱstrN-H,-OH) 2889 arom C-H) cm −1 conforming the tosylation of Microcrystalline Cellulose (C TOS ) [33]. Solubility of the prepared tosylated Cellulose (C TOS ) was observed. Obtained tosylated Cellulose (C TOS ) was soluble in aprotic highly polar organic solvents (DMSO) and was insoluble in a lot of protic or polar solvents (like water, Ethanol). Elemental analysis was helpful for finding the degree of substitution by finding out the percentage of the elements found in the sample. Using Sulfur content in the samples Degree of substitution (number of hydroxyl groups substituted per Glucose unit) was carried out using the formula [10]. 1 HNMR (solution of C TOS in DMSO-d 6 ) shows the tosyl group hydrogens appear as two broad and two sharp peaks for the benzene ring between 7 and 8 ppm 7.75 CH, 7.35 CH and methyl group CH 3 appears at 2.42 ppm [5]. Peaks for the Cellulose, which are between 3.5 to 5.5 ppm, are for the cellulose polymer backbone. The intensity of the 1 HNMR for tosylate group covalent bond to Microcrystalline cellulose backbone was not very high in earlier attempts, suggesting that DS TOS is less, meaning not all the hydroxyl groups can be substituted; rather, degree of substitution depends on the ratio of Tosyl Chloride to Cellulose in reaction mixture. Keeping this in mind, we modified the method previously reported to obtain the tosylated cellulose up to 0.5 DS. Degree of substitution was also responsible on the solubility of the Tosyl Chloride and the products formed [34]. Solubility is prerequisite for further reaction and characterization such as 1 HNMR. Tosylated cellulose with DS TOS more than 0.43 are DMSO soluble; upon DS TOS 0.95, it is further soluble in aprotic solvent in DMSO, DMA and DMF. Tosylated cellulose was prepared following Rahn et al.'s synthetic method of dissolving Microcrystalline Cellulose in DMA/LiCl; having DS TOS , 0.46 are soluble in DMF, DMSO and DMA [29]. Our lab-synthesized Tosylated Cellulose was DMF soluble. No hints of any side reaction were found.

Synthesis of Microcrystalline Cellulose Amine Derivatives
Tosylated cellulose (C TOS ) was converted to amine cellulose derivatives by stirring tosylated cellulose with corresponding amines in a 1:25 per anhydroglucose unit (AGU) mole ratio. Excess amount of amine (1:25) ratio was used to avoid any side reaction and crosslinking and obtain a soluble product [18,28]. Reaction was preceded for 5 h at 100 • C in DMF as reported for tosylated group replacement by many amines to form 6-deoxy-6-substituted amine cellulose derivatives. Amine cellulose derivatives of C TOS are regioselective modification at position 6. Nucleophilic substitution is preferred at primary tosylated sites rather than secondary tosylated [35]. Nucleophilic substitution reaction is not quantitative in all reactions [36], and because of polymer chemistry, it is impossible to remove the tosyl group as in case of other organic compounds of lower molecular weight. Reaction products of higher DS TOS microcrystalline cellulose also show unremoved tosyl groups from products as tosyl groups are present at position 2 of Microcrystalline cellulose [37].
In the present study, tosylated cellulose was reacted with Hydrazide, diethylamide and diethyl triamine. Yield of the aminated cellulose derivatives Cell Hyd, Cell DEA and Cell DETA was found to be 84%, 80% and 89%, respectively. Figure 1a shows the FTIR spectra as compared to the Microcrystalline Cellulose. From these spectra, it is indicated that the amines have been substituted on the Microcrystalline Cellulose backbone. FTIR spectra of aminated Cellulose derivatives were in accordance with already reported data as described by [38].
bonded to the cellulose while dimethylamines N-H participated in bonding as shown in the Figure  2. It is quite attractive to mention that C-H stretching band has shifted to a higher wavenumber value from 2899 cm −1 along with the increase in intensity of CH2 bending band from 1428 cm −1 resulting in Cell derivatives that are more crystalline as compared to the CTOS [20]. N-H wag appears (primary and secondary amines only) from 910-665 cm −1 .

Tosylation of Cellulose
Dried microcrystalline Cellulose MCC, 10 g (61.6 mM of anhydrous glucose unit (AGU)) was taken in 1000 mL flask, and 250 mL of N,N-Dimethyl acetamide synthetic grade (DMA) was added and stirred at 120 °C for 1 h. Resulting slurry was cooled to 100 °C, and then, Lithium Chloride Anhydrous LiCl, (20 g) in DMA (50 mL), was added dropwise. Stirring was continued overnight until the complete dissolution of the Cellulose. A volume of 37.2 mL of Triethylamine (TEA) (370 mM), 6 mol/AGU in 20 mL of DMA, was added to the cellulose solution at constant stirring for half hour. The solution temperature was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl chloride (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was continued on stirring for 24 h, and color of the mixture changed from yellow to dark orange. Homogenous mixture was poured into ice water. Precipitates were collected by filtration and then washed by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and recollected in deionized water. After filtration, it was washed with Ethanol (500 mL × 3). Tosylated Cellulose obtained was dried below 50 °C in oven.

Tosylation of Cellulose
Dried microcrystalline Cellulose MCC, 10 g (61.6 mM of anhydrous glucose unit (AGU)) was taken in 1000 mL flask, and 250 mL of N,N-Dimethyl acetamide synthetic grade (DMA) was added and stirred at 120 °C for 1 h. Resulting slurry was cooled to 100 °C, and then, Lithium Chloride Anhydrous LiCl, (20 g) in DMA (50 mL), was added dropwise. Stirring was continued overnight until the complete dissolution of the Cellulose. A volume of 37.2 mL of Triethylamine (TEA) (370 mM), 6 mol/AGU in 20 mL of DMA, was added to the cellulose solution at constant stirring for half hour. The solution temperature was dropped from room temperature to 3-8 °C, and p-Toluene sulfonyl chloride (70.6 g, 369.6 mM, 6 mol/AGU dissolved in 50 mL of DMA) was added slowly. Reaction was continued on stirring for 24 h, and color of the mixture changed from yellow to dark orange. Homogenous mixture was poured into ice water. Precipitates were collected by filtration and then washed by deionized water (8 L) and 1 L of ethanol, suspended in 500 mL of boiling acetone and recollected in deionized water. After filtration, it was washed with Ethanol (500 mL × 3

Materials
All chemicals and reagents, viz.  1570 cm −1 , CH 2 symmetric and asymmetric bending at1471 cm −1 1312 cm −1 , C-N for aliphatic amine appeared at 1160 cm −1 along with the signature peaks of Microcrystalline Cellulose. As mentioned in the literature [39], primary amines show overtone between 1590-1650 cm −1 while secondary amines show overtone at 1550 to 1650 cm −1 . This strengthens the idea that one of the NH 2 of hydrazine and triethylamine is bonded to the cellulose while dimethylamines N-H participated in bonding as shown in the Figure 2. It is quite attractive to mention that C-H stretching band has shifted to a higher wavenumber value from 2899 cm −1 along with the increase in intensity of CH 2 bending band from 1428 cm −1 resulting in Cell derivatives that are more crystalline as compared to the C TOS [20]. N-H wag appears (primary and secondary amines only) from 910-665 cm −1 . 1 HMNR spectra of the 6-deoxy-6-substituted amine/aminated cellulose in DMSO-d6 are represented in Figure 1c) Microcrystalline cellulose backbone aromatic ring hydrogens peaks appeared between 3 to 5.3 ppm [40]. For Cell Hyd, along with the MCC backbone peaks, single H of NH appeared sharply at 6.2, while NH2 Hydrogen expected to appear at 3.23 ppm. In case of Cell DEA [41] along with MCC peaks, CH2 multiplet and CH3 triplet appeared at 2.59 and 1.15 ppm, respectively, evidencing the successful substitution on cellulose. For Cell DETA along with MCC back bone, NH2 singlet appeared at 1.03, multiplet for CH2 Hydrogen appeared at 2.59-2.69 ppm, NH hydrogen signal appeared at 1.77 ppm, and at 3.7 ppm, there was broad signal for NH, respectively.
From the 1 HMNR data, it is clear there is complete removal of the ionic tosyl moieties from all the Cellulose amine derivatives. From the spectra, it is clear there was successful reaction between the tosylated cellulose and amines, resulted by removal of the one hydrogen from the primary amine NH2 or secondary amine NH and bonding with the position 6 methylene group of MCC as is 1 HMNR spectra of the 6-deoxy-6-substituted amine/aminated cellulose in DMSO-d6 are represented in Figure 1c Microcrystalline cellulose backbone aromatic ring hydrogens peaks appeared between 3 to 5.3 ppm [40]. For Cell Hyd, along with the MCC backbone peaks, single H of NH appeared sharply at 6.2, while NH 2 Hydrogen expected to appear at 3.23 ppm. In case of Cell DEA [41] along with MCC peaks, CH 2 multiplet and CH 3 triplet appeared at 2.59 and 1.15 ppm, respectively, evidencing the successful substitution on cellulose. For Cell DETA along with MCC back bone, NH 2 singlet appeared at 1.03, multiplet for CH 2 Hydrogen appeared at 2.59-2.69 ppm, NH hydrogen signal appeared at 1.77 ppm, and at 3.7 ppm, there was broad signal for NH, respectively.
From the 1 HMNR data, it is clear there is complete removal of the ionic tosyl moieties from all the Cellulose amine derivatives. From the spectra, it is clear there was successful reaction between the tosylated cellulose and amines, resulted by removal of the one hydrogen from the primary amine NH 2 or secondary amine NH and bonding with the position 6 methylene group of MCC as is evidenced by FTIR. In case of Cell Hyd, one Hydrogen of hydrazine NH 2 was replaced by bonding with methylene of MCC; thus, single Hydrogen of NH appeared sharply at 6.2, and second hydrazine NH 2 Hydrogen expected to appear at 3.2 ppm was masked under the area of Cellulose backbone hydrogens. For Cell DEA, there was no peak for NH observed, suggesting the bonding occurred between Nitrogen and methylene of MCC. Cell DETA synthesis via primary amine NH 2 and methylene carbon was vivid from the broad peak at 3.7 ppm (masked by Cellulose backbone peaks area), multiples of CH 2 hydrogen at 2.59-2.69 and appearance of NH Hydrogen at 1.77. Appearance of some of the tosylated moieties attached to the cellulose backbone as two broad and two sharp peaks for the benzene ring between 7 and 8 was very low as reported by Heinze T et al. [5]. This can be attributed to the steric hinderance of the amine groups of DEA and the polymeric structure of Cellulose resulting in less Degree of Amination. 13 CNMR no detectable peaks of tosyl group between 128 to 140 ppm were found while there were high intensity peaks for CH 2 NH 2 appeared around 52 and 57 ppm while the methyl and methylene Carbons next to Hydrogen appeared between 45 to 35 ppm.
Elemental analysis was carried out for the DS TOS and DS Amine . Degree of amination was found to be 0.40 to 0.43, suggesting that the maximum number of tosyl group has been removed. Elemental analysis data in Table 1 proved that there is no chlorine moiety resulting from a side product. No polymer degradation resulted in the synthesis reaction. Yield of the reactions was more than 80%. In all the derivatives, a trace amount of sulfur of 0.5%, 1.01% and 0.77% for Cell Hyd, Cell DEA and Cell DETA was found, respectively. Complete removal of Tosyl group was not possible because of the polymeric structure of the Cellulose, but Nitrogen content of 8.26%, 3.68% and 9.55% in case of Cell Hyd, Cell DEA and Cell DETA was found, respectively, of the derivatives, which was quite high, reflecting the substitution of the Tosyl group and modification of cellulose backbone by amines. To analyze the effect of the amine modifications on cellulose backbone, the crystal structure of the cellulose and its aminated Cellulose derivatives was observed with wide angle powder X-ray diffractogram shown in Figure 1b. From the data, it was possible to evaluate qualitatively that microcrystalline cellulose has the diffraction pattern of semi crystalline cellulose type I, [ [30,43]. The diffraction pattern of the cellulose changed as reported in previous studies [26] after the tosylation and derivatization indicating that all the chemical modification dissolution of Cellulose [44] in LiCl/DMA/TEA affected the lattice and changed the crystallinity of the cellulose as appeared from reasonable lowering of the peak intensity. C TOS displayed a broad peak at 2θ = 20 • (021) of amorphous cellulose II [33,45]. All aminated Cellulose derivatives (Cell Hyd, Cell DEA and Cell DETA) show decrease in the crystallinity as evident from the low peak heights [46] and more of amorphous structure as reported by others [17]. Decrease in crystalline structure from starting Microcrystalline Cellulose during functionalization is because of the disturbance of cellulose chains inter and intramolecular hydrogen bonding [47][48][49]. This indicated the correlation between the findings of the FTIR, 1 HNMR and elemental analysis. Several other researchers [50,51] also mentioned the intense hydrogen bonding responsible for the crystalline part of cellulose, so loss of OH group is responsible for decrease in crystalline structure. From the Cell Hyd, Cell DEA and Cell DETA diffraction spectra, peaks at diffraction angles 2θ = 20.  [52]. It is interesting to mention that the amine cellulose derivatives have higher peak height meaning crystallinity than the C TOS indicating that the nucleophilic substitution of the Tosyl group by amines have resulted into products with increased the number of unreacted OH and NH moieties available for inter and intramolecular hydrogen bonding leading to in increased ordered compact arrangement. It is quite intriguing to mention that the XRD pattern are quite convincing with already reported work [53]. Increasing randomness of the amorphous phase in the cellulose amine derivatives caused long range spacing of polymeric chains resulting in the decrease in crystalline structure as reported elsewhere [54].
Zeta potential ζ of the cellulose and its amine cellulose derivatives was measured as shown in listed in Table 2 at neutral Ph. From Figure 1d, we observed all the derivatives shifted to a positive value of zeta potential from a negative zeta potential of cellulose as reported elsewhere [55]. Aminated cellulose derivatives expressed cationic character in aqueous solution. Zeta potential values showed a very minor change after incubation for several hours at 37 • C showing stable zeta potential values. Zeta potential values helped in the confirmation of the modification of the microcrystalline cellulose. Positive zeta potential values are because of the protonation of the amine groups. On comparing the zeta potential values of the cellulose, amine derivatives increased number of primary amino groups resulted in more positive zeta potential values [56]. Positively charged amine derivatives foster muco-adhesion resulting in increased residence time on mucosa, which is absent in the native Microcrystalline cellulose. This kind of bio-adhesion is very important in case of biomedical application. Cellulose derivatives exhibiting positive charge due to secondary amine structure have been reported in previous studies [57].
SEM micrographs helped in understanding the effects of all the modification on surface morphology. Microcrystalline Cellulose (MCC) exhibits the homogeneous structure of the fibers having a well oriented network like structure (Figure 3), while C TOS showed a sheet-like heterogenous structure with rough surface interconnected to form porous structures. This indicates the loss of cellulose surface order after chemical modification [58]. For aminated cellulose derivatives, we see that the interconnected structure of fibers and some rough surface and sheet like porous structure appear indicating the presence of the tosyl group and amine moieties on the surface of the aminated cellulose derivatives as indicated by the 1 HNMR [27].
SEM structure of the chemically modified microcrystalline cellulose fiber has become rough surfaced small fibers and particles rather than the clear smooth ones because during the modification, Microcrystalline cellulose has undergone swelling, new crystal structural modification with addition of the functional groups as predicted by the XRD structure [59]. Similarity type of the irregular rod like rough structure between the microcrystalline cellulose and aminated cellulose, indicating that there was homogenous amination of the polymer without much alteration of surface morphology [48]. Another useful information was acquired by EDX data as shown in Figure 3. The EDX spectra reinforced the data from Elemental Analysis by showing the presence of Nitrogen in the aminated Cellulose Derivatives in enough quantity to prove the successful synthesis of the aminated Cellulose derivatives from Microcrystalline Cellulose (MCC) via tosylation reaction.
Swelling ratios of the Cellulose and its aminated cellulose derivatives are important because these help in understanding the solute diffusion as well as surface properties of the compounds. Figure 4f shows the swelling ratios in PBS. Cellulose showed the highest swelling ratio at 69 ± 2, which decreased in all other aminated cellulose derivatives. This relatively high cellulose swelling ratio is because of the penetration of the water in amorphous regions of cellulose causing changes in the crystal structure of the cellulose from Cellulose I to Cellulose II as corroborated by XRD. Aminated Cellulose derivatives, because of presence of the NH 2 moieties with the cellulose backbone and disordered arrangements of the polymeric chains, caused the high swelling ratios 60.8 ± 1, 50 ± 2 and 59.8 ± 3 for Cell Hyd, Cell DEA and Cell DETA, respectively.  selective cytotoxic behavior for cancer cells as compared to the normal cell line. The higher the values of SI, the more selective the compound is [65].
In another report of amine functional derivatives, carrying longer aliphatic chains on the nitrogen atom is superior to shorter ones in improving cytotoxicity [64]; a similar trend can be seen in our study of the difference in the metabolic rate inhibition effect of Cell Hyd compared to Cell DETA.

Live Dead Assay
Live/dead assay was performed to confirm the cytotoxic behavior of the aminated cellulose derivatives towards the cancer cell lines and fibroblast cell lines. Cells were treated with the IC50 value (derived from Table 3) and a value higher than IC50 (250 μg/ml) and a value lower than IC50 value (20 μg/ml) results to visualize the effect of the compounds on the cancer cell lines. Fluorescent visualization of live and dead cells is shown in Figure 5. Live cells are detected as green fluorescence by Calcein indicating intracellular esterate activity, and dead cells are detected as red fluorescence when ethidium homodimer binds to DNA. Ethidium homodimer is excluded from live cells because of cell membrane integrity, while in dead cells, loss of plasma membrane activity allows ethidium homodimer entering cells and binding to DNA. Live/Dead Assay revealed the live/dead cells proportion in the culture medium. It is clear from Figure 5 that the amine functionality gives aminated cellulose derivatives cytotoxic ability and causes arrest of cell proliferation. Moreover, the

Cytotoxicity
Cellulose amine derivatives have been evaluated against bacteria in many reports, but there has been less attention given to the cytotoxicity. To ensure the use of cellulose amine derivatives in biomedical applications, it is very important to explore the cytotoxicity of these materials as a first step. Literature survey showed Finger S et al. reported 6-deoxy-6aminoethyleneamino cellulose with different degree of substitution (DS) via tosylation against keratinocyte cell (HaCaT). Their studies concluded that lowest DS (0.3) was most biocompatible with (HaCaT) [60]. While in another study, El-Sayed et al. carried out cytotoxic studies against BJ1 of 3-aminopropyltrimethoxysilane and TiO 2 grafted tosylated cellulose. TC DS TOS = 0.77, TC-Si, TC-Si/TiO 2 were prepared. TC TC-Si showed moderate cytotoxicity by 17% and 23.8% while TC-Si/TiO 2 enhanced the proliferation of BJ1 by 42% [26]. In this study, novel MCC derivatives Cell Hyd, Cell DEA and Cell DETA have DS amination 0.40-0.43. The abovementioned studies encouraged us to further explore and investigate cellulose derivatives interaction with cell lines. Breast cancer is the second most deadly cancer in the US. Melanoma is a cancer that occurs in cells (cutaneous, mucosal or ocular) responsible for formation of colored pigment melanin. Melanoma is the most abundant cancer affecting those between 25 to 29 years in the USA. These most common skin cancers representing cell lines were used for the cytotoxic study against aminated cellulose derivatives.
The ability of the synthesized aminated cellulose and microcrystalline cellulose to inhibit the metabolic activity of the cancerous B16F10 (mouse skin melanoma), MDA-MB-231 (human epithelial adenocarcinoma) and MCF-7 (human breast lines adenocarcinoma) and non-cancerous cell lines NIH3T3 fibroblasts was evaluated by standard Presto blue assay for cell viability. Presto blue reagent was used to measure viability of cells. Presto blue reagent (Resazurin) was reduced to resorufin by metabolically active cells indicating mitochondrial activity of the living cells. Nontreated cells were used as control, and cytotoxic activity of compounds was evaluated as the concentration of compounds inhibiting 50% of already grown cells (IC 50 ) after 24h using Prestoblue assay listed in Table 3. To ensure the proper solubility of the derivatives, amines were first dissolved in DMSO and then were diluted to DMEM + 10%FBS + 1% Penicillin; since the maximum concentration of DMSO was not more that 2%, DMSO cytotoxicity was limited. Cytotoxicity of the compounds was evaluated by adding serial diluted concentrations of amine functionalized compounds to cells seeded in 96-well plate. IC 50 (the half maximal inhibitory concentration) value of the compounds was calculated by dose-response curves determined from the cytotoxicity assay by plotting IC 50 curves shown in Figure 4a-d. Interestingly, all aminated cellulose derivatives exhibited good metabolic inhibiting activity against cancer cell lines (B16F10, MDA-MB-231 and MCF-7) as compared to normal NIH3T3 cells listed in Table 3. Based on IC 50 , values of pure cellulose were not cytotoxic at lower concentrations for all cell lines, and IC 50 values are highest for NIH3T3 263.9 µg/mL while 207, 201.6 and 238.9 µg/mL are for B16F10, MDA-MB-231 and MCF-7, respectively. For cancer cell lines, IC 50 values ranged between 75 µg/mL and 205 µg/mL for aminated cellulose derivatives as shown in Figure 4e. Cell DEA and Cell DETA displayed higher anticancer activity as compared to Cell Hyd for melanoma and breast cancer cell lines as shown in Figure 4e. Cell DETA showed promising results against B16F10 (mouse skin melanoma) (IC 50 < 101.5 µg/mL) and MCF-7 (human breast adenocarcinoma) cell line (IC 50 < 74.92 µg/mL) while Cell DEA was more cytotoxically potent against MDA-MB-231 (human epithelial adenocarcinoma) (IC 50 < 154.6 µg/mL). All compounds showed excellent metabolic inhibiting results against B16F10 (mouse skin melanoma) Cell Hyd 130.5 µg/mL, Cell DEA103.64 µg/mL and Cell DETA 101.5 µg/mL. Same serial gradient concentrations used against cancer cell lines were screened against fibroblast NIH3T3 cell lines for selective cytotoxicity comparison. For fibroblast cells, safe concentration values were up to 231 µg/mL, 222 to 260 µg/mL for Cell Hyd, Cell DEA and Cell DETA, respectively, after that cells metabolic activity decreased. Microcrystalline Cellulose was not found cytotoxic. Abercrombie et al. reported that cancer cells may have slightly elevated negative surface charge on the cell membrane than normal cells [61]. The low metabolic activity in cancer cells is due to interaction of positive potential (zeta potential) on aminated cellulose derivatives with negative charge on cell membrane [55,62]. Thus, depolarization of membrane and imbalance in ionic transport occurred [63]. An alteration in cell signal stimulates the mitochondria to generate intracellular oxidation stress, thereby decreasing metabolic activity of cells. The significant difference in the cytotoxicity of Cell DETA could be attributed to the synergistic effect of surface potential and long chain aliphatic group on tertiary amine.
Primary amine derivatives as compared to the tertiary amine derivatives showed considerable growth inhibitory activity to the cancer cell lines as compared to fibroblast cell line. It can be seen vividly that the compounds are moderately selective towards cancer cell lines over normal cell lines. Recently, Cheng et al. developed amine functionalized anticancer drugs, and they had more selectivity between normal and cancer cells [64]. Comparing the IC 50 values of the normal cell line and the cancer cell line, Selectivity Index can be calculated. SI is useful as indicator of the compound's selective cytotoxic behavior for cancer cells as compared to the normal cell line. The higher the values of SI, the more selective the compound is [65].
In another report of amine functional derivatives, carrying longer aliphatic chains on the nitrogen atom is superior to shorter ones in improving cytotoxicity [64]; a similar trend can be seen in our study of the difference in the metabolic rate inhibition effect of Cell Hyd compared to Cell DETA.

Live Dead Assay
Live/dead assay was performed to confirm the cytotoxic behavior of the aminated cellulose derivatives towards the cancer cell lines and fibroblast cell lines. Cells were treated with the IC 50 value (derived from Table 3) and a value higher than IC 50 (250 µg/mL) and a value lower than IC 50 value (20 µg/mL) results to visualize the effect of the compounds on the cancer cell lines. Fluorescent visualization of live and dead cells is shown in Figure 5. Live cells are detected as green fluorescence by Calcein indicating intracellular esterate activity, and dead cells are detected as red fluorescence when ethidium homodimer binds to DNA. Ethidium homodimer is excluded from live cells because of cell membrane integrity, while in dead cells, loss of plasma membrane activity allows ethidium homodimer entering cells and binding to DNA. Live/Dead Assay revealed the live/dead cells proportion in the culture medium. It is clear from Figure 5 that the amine functionality gives aminated cellulose derivatives cytotoxic ability and causes arrest of cell proliferation. Moreover, the higher concentrations of Cell Hyd, Cell DEA and Cell DETA not only kill the maximum cancer cells within 24 h but, at the same time, their high concentration becomes cytotoxic for the normal cell lines.
Live dead assay results suggested that at IC 50 values the morphology of the cells have changed as compared to the (20 µg/mL). Cells are making round morphologies and are detached from each other losing their intercellular network. Cells showed the shrinkage in size one of the fundamental characteristics of apoptosis [66]. Moreover MCF-7 cells showed the cluster formation. Cytotoxicity was also observed by Image J software on the live dead cell images. Percentage of viable cells found from Image J has been shown in Figure 5. Overall, the cells in the (20 µg/mL) were showing more than 91% cell viability while in the presence of aminated cellulose derivative at IC 50 , we can see the live cell percentage is decreasing significantly by 50 percent in cancer cells after 24 h, as reported elsewhere [67]. All compounds had high cytotoxicity against B16F10 cell lines. MDA-MB-231 showed almost same vulnerability to Cell DEA and Cell DETA. While Cell DETA is very effective against the MCF-7 cell lines. In Live dead assay images, NIH3T3 cells have good morphology and intercellular network suggesting non cytotoxic to normal cell lines under 200 µg/mL. This suggests that in safe concentration, Cell Hyd, Cell DEA and Cell DETA can be used for tissue engineering applications in further studies.

Conclusions
MCC aminated derivatives Cell Hyd, Cell DEA and Cell DETA were successfully synthesized by tosylation intermediate with DS amination 0.40-0.43. Cell Hyd, Cell DEA and Cell DETA have C-N peak 1160-1170 and N-H peak between 3200 cm −1 . 1 HNMR confirmed the successful synthesis of cellulose derivatives. Dissolution and chemical modification affected the inter and intra molecular hydrogen bonding thus Cell Hyd, Cell DEA and Cell DETA have decreased crystallinity as compared to MCC in XRD and SEM. MCC was non cytotoxic for cell lines whereas positive zetapotential values of Cell Hyd, Cell DEA and Cell DETA were responsible for the selective cytotoxicity for Melanoma and Breast Cancer cell lines as compared to fibroblast cell lines (NIH3T3). The mouse skin melanoma (B16F10) is the most sensitive cells to the cytotoxic effects of Cell Hyd, Cell DEA and Cell DETA, followed by human breast adenocarcinoma (MCF-7). Cell Hyd, Cell DEA and Cell DETA are safe up to 200 µg/mL for the fibroblast cell lines (NIH3T3). Live/Dead assay provided the assessment that live/dead cells proportion at IC 50 is almost 50%. Based on the abovementioned results, we can conclude that, Cell Hyd, Cell DEA and Cell DETA proved to be a practical candidate for further study as biocompatible scaffold in tissue engineering applications, on one hand, while on the other hand, effective anticancer agent in cancer therapeutics.