Chitosan Coated Luteolin Nanostructured Lipid Carriers: Optimization, In Vitro-Ex Vivo Assessments and Cytotoxicity Study in Breast Cancer Cells

: In the present study, luteolin (LTN)-encapsulated chitosan (CS) coated nanostructured lipid carriers (NLCs) were formulated using the melt emulsiﬁcation ultrasonication technique. NLCs were optimized by using the 3 3 -QbD approach for improved in vitro efﬁcacy against breast cancer cell lines. The optimized LTN-CS-NLCs were successfully characterized by different in vitro and ex vivo experiments as well as evaluated for cytotoxicity in MDA-MB-231 and MCF-7 cell lines. The prepared LTN-CS-NLCs showed particle size (PS), polydispersity index (PDI), and entrapment efﬁciency (%EE) in the range between 101.25 nm and 158.04 nm, 0.11 and 0.20, and 65.55% and 95.37%, respectively. Coating of NLCs with CS signiﬁcantly increased the particle size, encapsulation efﬁciency, and zeta potential changes positively. Moreover, slow-release rate of LTN was achieved during 24 h of study for LTN-CS-NLCs. In addition, optimized LTN-CS-NLCs showed signiﬁcantly higher mucoadhesion, gastrointestinal stability, and intestinal permeation compared to non-coated LTN-NLCs and LTN suspension. Furthermore, LTN-CS-NLCs showed statistically enhanced antioxidant potential as well as dose and time-dependent cytotoxicity against MDA-MB-231 and MCF-7 cells compared to uncoated LTN-NLCs and pure LTN. On the basis of the above ﬁndings, it may be stated that chitosan-coated LTN-NLCs represents a great potential for breast cancer management. by of LTN in lipid the


Introduction
Breast cancer (BC) is the most frequently diagnosed solid tumor and the second leading cause of cancer death after lung cancer. Among women, breast cancer accounts for almost 30% of all newly diagnosed cancer cases [1,2]. The uncontrolled malignant cell growth at the inner lining of breast ducts leads to the development of BC. Age, sex, breast condition, estrogen level, and family history are the major factors related to a higher risk for the development of BC [3]. Furthermore, postmenopausal women are considered to have more risk. Up to 7 per cent of breast cancers are diagnosed in women under 40 years of age and less than 4 per cent in women under 35 years of age [4]. At present, Table 1. Various independent and dependent variables used in the Box-Behnken design for the preparation of chitosan coated luteolin nanostructured lipid carriers (LTN-CS-NLCs).

Formulation of LTN-CS-NLCs
LTN-CS-NLCs were formulated by the melt emulsification ultrasonication technique as per the reported procedure with slight modification [21]. Glyceryl monostearate (solid lipid; melting point: 66 • C) and Capryol 90 (liquid lipid) were selected to make the lipid matrix. Accurately weighed lipid (X 1 ; 2-4% w/v) was melted at 70 • C and LTN (20 mg) was added to prepare homogeneous and uniform lipid phase. The aqueous phase was prepared with P-188 (as a surfactant; X 2 ; 1-2% w/v), and TPGS (0.25% w/v as a stabilizer) in 10 mL of previously prepared 0.2% w/v CS and heated to the same temperature. CS solution (0.2% w/v) was prepared by dissolving 20 mg of CS in 10 mL of 1% acetic acid solution (pH 5.0) with continuous stirring for 30 min. The surfactant solution was added dropwise to the melted lipid phase with constant stirring at 750 rpm. The prepared sample was stirred for 30 min to get a transparent emulsion. In the end, the obtained transparent emulsion was further probe sonicated (Hielscher, Ultrasound UP-50 H, Teltow, Germany) (X 3 ; 3-5 min) to obtain nanosized NLCs. LT-NLCs were prepared with the same composition and condition without the addition of chitosan (CS).

Particle Characterization
The prepared LTN-CS-NLCs and LTN-NLCs were characterized for PS, PDI, and zeta potential (ZP). The size of diluted samples (100 fold) were measured in zeta sizer (Malvern Instruments, Worcestershire, UK). ZP of optimized nanoparticles was assessed to determine the charge on NPs surface. The surface morphology of selected LTN-CS- NLCs and LTN-NLCs was evaluated on transmission electron microscope (TEM, JEO-1010, Tokyo, Japan)) at 160 kV voltage. The samples were stained with phosphotungstic acid and visualized under the microscope at high resolution. The micrographs were captured and visualized with the help of imaging viewer software.

Entrapment Efficiency (%EE) and Drug Loading (%DL)
%EE and %DL of optimized LTN-CS-NLCs and LTN-NLCs were determined by the direct method as per the reported procedure with slight modification [18]. Free LTN was collected after precipitation of the NPs using acetonitrile, followed by centrifugation at 20,000 rpm for 10 min at 4 • C. The pellets containing the entrapped LTN were dissolved in dimethylsulfoxide (DMSO) and methanol solution in the ratio of 1:1 and heated at 70 • C. The quantity of LTN encapsulated within the NLCs matrix was determined by UV spectrophotometer (Shimadzu 1700, Shimadzu Corp., Kyoto, Japan). The %EE and %DL of prepared NLCs were calculated by the following equations:

In Vitro Gastrointestinal Stability Study
The selected optimized LTN-CS-NLCs was evaluated for gastrointestinal stability as per the published procedure [22,23]. The stability in simulated intestinal fluid (SIF) and gastric fluid (SGF) was assessed. SGF was prepared by dissolving 100 mg of pepsin in 5 mL of water containing 0.35 mL concentrated HCl followed by the addition of sodium chloride (100 mg) and volume adjustment (up to 50 mL) with water. Finally, the pH of the solution was modified to 1.2 by the addition of concentrated HCl. SIF was prepared by dissolving 340 mg of monobasic potassium phosphate in 10 mL of water followed by the addition of 3.85 mL of 0.2 M NaOH and 500 mg of pancreatin. Finally, the volume was increased to 50 mL, and the pH was adjusted to 6.8 by NaOH [22]. LTN-CS-NLCs (0.1 mL) were withdrawn and diluted up to 5 mL (1 in 50) in SIF and SGF and incubated at 37 • C. At a specific time (0, 2, 4, 8, 12 h) the sample was evaluated for PS, PDI, EE, and surface morphology.

LTN Release Study
LTN release study was performed for LTN-CS-NLCs, LTN-NLCs, and LTN suspension (control) in release medium SIF (900 mL, pH 6.8) at 37 • C. Optimized LTN-CS-NLCs and LTN-NLCs (~5 mg of LTN) was placed in the dialysis bag (MW 12,000 g/mole) and dipped into release medium with stirring speed of 100 rpm. At a specific time point, the released content (5 mL) was withdrawn and replaced with the same volume. The collected samples were filtered, diluted, and analyzed to quantify LTN content using UV spectrophotometer (Shimadzu 1700, Shimadzu Corp., Kyoto, Japan). Further, the released data was fitted into various kinetic models to analyze the mechanism of LTN release [24].

Mucoadhesion Study
The optimized LTN-CS-NLCs, LTN-NLCs, and LTN suspensions were evaluated for mucoadhesion study to check the adsorption of mucin on the NLCs [25]. The mucin solution (1 mg/mL) was prepared and mixed with the prepared formulations in 1:1 ratio. The mixture was incubated at 37 • C for 2 h and then centrifuged at 13,000 rpm for 60 min. The supernatant was taken, diluted appropriately, and analyzed spectrophotometrically (Shimadzu 1700, Shimadzu Corp., Kyoto, Japan) at 258 nm to calculate the free mucin content. The formula used to calculate as given below [26].
where C 0 = initial mucin content and C f = free mucin content.

Antioxidant Activity
The study was performed for optimized LTN-CS-NLCs, LTN-NLCs, and LTN suspension to check the antioxidant potential by the reported procedure with slight modification [27]. The stock solution (10 mg/mL) was prepared for all three samples in ethanol and further diluted to make the concentration of 25-250 µg/mL. All the samples (500 µL) were taken and transferred to 2,2-diphenyl-1-picrylhydrazyl (DPPH) solution (0.02% in ethanol). The samples were shaken for complete reaction and placed in the dark at 25 • C for 1 h. The reaction took place between violet color DPPH and antioxidants. The violet color of the solution turns colorless after the completion of the reaction. Similarly, this experiment was repeated for placebo NLCs. The samples were examined spectrophotometrically (Shimadzu 1700, Shimadzu Corp., Kyoto, Japan) at 517 nm, and calculation was done using the formula: Radical Scavenging (%) = Absorbance of control − Absorbance of test Absorbance of control × 100

Cytotoxicity Study
MTT assays of LTN-CS-NLCs, LTN-NLCs, and LTN suspension were performed to check the per cent cytotoxicity [28]. This test works on the mechanism of the formation of yellow tetrazolium salt to insoluble purple formazan crystals [29]. Both MDA-MB-231 and MCF-7 cells were seeded 24 h before the study. The cell counts 1 × 10 5 /well were taken for the study, and different concentrations of each sample were incubated for 48 h and 72 h, respectively. After that, cells were incubated with MTT (20 µL, 5 mg/mL in phosphate buffer saline-PBS) in a fresh medium for 4 h under CO 2 incubator. The formed formazan crystal was solubilized in DMSO (150 µL/well). The absorbance was noted at 570 nm on a microplate reader (Bio Tek Instruments, Mumbai, India).

DAPI for Nuclear Staining
MDA-MB-231 and MCF-7 cells (10 5 cells/well) were cultured, treated with LTN-CS-NLCs as well as LTN-NLCs, and incubated for 48 h. Following incubation, DMSO control and treated cells were washed twice with PBS and fixed in glutaraldehyde (2.5%) for 20 min. Subsequently, the cells were permeabilized in Triton X-100 (0.1%) for 15 min and stained with DAPI (4 ,6-diamidino-2-phenylindole) for 20 min in the dark. After being washed 3 times with PBS, the nuclear morphology of cells was observed by fluorescence microscopy (Olympus, Japan) [30].

Intestinal Permeation Study
The permeation experiment of LTN-CS-NLCs, LTN-NLCs, and LTN suspension was conducted to determine the amount of drug permeated at specific times. The study was performed on the goat intestine by the reported procedure with slight modification [31]. The fresh goat intestine was collected from the local slaughterhouse at an abattoir in a sterile beaker and washed with Kreb's solution to remove the food residues. The formulations (~5 mg of LTN) were carefully placed in the intestinal sac, and both ends were ligated tightly. The samples were placed in a beaker containing Kreb's solution (250 mL) and regularly oxygenated with 95% oxygen using an aerator. The released content (2 mL) was taken at a specific time point and replaced with the same volume. The samples were filtered, diluted, and quantified by using UV spectrophotometer (Shimadzu 1700, Shimadzu Corp., Kyoto, Japan). The permeation flux and apparent permeability coefficient (APC; P app ) and were determined for the formulations by the following equation.

Statistical Analysis
Experiments were conducted 3 times, and their findings were represented as average ± SD. Statistical analysis was performed with GraphPad Prism (version 7). Furthermore, the data were analyzed statistically using ANOVA and Tukey's test with the help of GraphPad Prism, version 7. The differences were considered significantly or highly significantly different from the control group when p < 0.05 and p < 0.01, respectively.

Optimization
The developed LTN-CS-NLCs were statistically optimized with 3 3 -Box-Behnken design. The impact of independent variables (X 1 , X 2 , and X 3 ) was evaluated on the dependent variables (Y 1 , Y 2 , and Y 3 ) using 3D response surface plot and contour plot ( Figure 1). Polynomial equations are used to assess the individual as well as the combined impact of all three independent variables. The quadratic model is the ideal model for the selected variables to show the effect individually as well as combinedly.
The independent variables lipid (% w/v, X 1 ); P-188 (% w/v, X 2 ) and ST (min, X 3 ) were taken at three levels {low (−1), medium (0), and high (+1)} to optimize LTN-CS-NLCs. The concentration range taken to develop LTN-CS-NLCs as lipid (X 1 ) as 2% (−1) to 4% (+1), P-188 (X 2 ) as 1% (−1) to 2% (+1) and ST 3 min (−1) to 5 min (+1). The design represented 15 formulations with 3 center points to analyze the error in the result of the same three compositions. The minimal PS (Y 1 ) was observed to be 101.25 nm (F14), and the maximal PS was observed to be 158.04 nm (F8). The PDI (Y 2 ) was obtained in the range of 0.115 (F2) to 0.201 (F12), and the %EE (Y 3 ) was obtained in the range of 65.55% (F14) to 95.37% (F8). The results obtained from the experiment, in other words, actual values, were observed to be much closer to the predicted values, as represented in Table 2. 3.1.1. Effect of Lipid (X 1 ), P-188 (X 2 ), and ST (X 3 ) on PS (Y 1 ) The polynomial equation indicating the relationship between the factors on PS (Y 1 ) is presented as follows: The impact of all three independent variables (X 1 , X 2 , and X 3 ) have been illustrated in the 3D and contour plots as depicted in Figure 1A. As per the polynomial equation and Figure 1A, a considerable impact of each independent variable on PS (Y 1 ) can be observed. Gradual increment in the PS was observed with the increase in lipid (X 1 ) concentration. As the lipid concentration increases the emulsifying capacity of surfactant decreases, which results in the aggregation of particles. The second variable P-188 (X 2 ) has depicted a negative impact of the PS. The increase in P-188 concentration from 1% to 2% w/v significantly (p < 0.05) decreases the PS. P-188 is a surfactant and stabilizer that significantly decreases the interfacial tension between lipid and aqueous phases, and helps to get small-sized emulsion [32]. At higher surfactant concentration, there was effective stability of NLCs achieved due to a steric barrier to the NLCs surface. It protects small NLCs particles by preventing aggregation [33]. Another probable elucidation for such reduction in the PS might happen from ST (X 3 ), which has a direct impact on PS. It helps to reduce PS during the development of LTN-CS-NLCs. The polynomial equation indicating the relationship between the factors on PDI (Y 2 ) is presented as follows:   The impact of all three independent variables (X 1 , X 2 , and X 3 ) has been illustrated in the response surface plot as depicted in Figure 1B. As per the polynomial equation and Figure 1B, a considerable impact of each independent variable was observed on PDI (Y 2 ). As the concentration of lipids (X 1 ) increased, PDI also significantly increased. The enhancement in PDI might be due to an increase in the heterogeneity of particles. Moreover, P-188 (X 2 ) showed a strong negative impact on the PDI. The surfactant significantly reduces the interfacial tension between the lipid and aqueous phase that leads to the development of uniform primary emulsion during the development of LTN-CS-NLCs. The third variable ST (X 3 ), is further responsible for an increase in the PDI due to the development of particles of different sizes. Table 2. Observed Box-Behnken experimental runs of LTN-NLCs with their actual and predicted experimental value.
The impact of all 3 independent variables (X 1 , X 2 , and X 3 ) has been illustrated in the response surface plot as depicted in Figure 1C. As per the polynomial equation and Figure 1C, a considerable impact of each independent variable on %EE (Y 3 ) was observed. The gradual enhancement in the %EE was observed with the increase in lipid (X 1 ) concentration. The increase in the lipid content provided more space for encapsulation of the drug into the lipid matrix [34]. Similarly, an increment in P-188 (X 2 ) concentration gradually improves the %EE. The increment in the concentration of P-188 led to an increase in the tendency of the drug to be entrapped in the lipid matrix resulting in improved %EE. Furthermore, with an increase in ST (X 3 ), %EE decreased significantly due to the reduction in PS.

Optimization by Point Prediction
The optimized LTN-CS-NLCs was selected on the criteria of small PS, PDI, and high EE among 15 compositions. Upon "trading off" different responses (Y 1 , Y 2 , and Y 3 ) using numerical desirability function, the optimized formulation composition (LTN-CS-NLCs) prepared with lipid (X 1 ; 3% w/v), P-188 (X 2 ; 2% w/v), and ST (X 3 ; 3 min) exhibited particle size of 123.84 ± 3.72 nm, PDI of 0.13 ± 0.01, and EE of 83.74 ± 4.68%, respectively. The software examined an analysis of variance (ANOVA) for all three responses (Y 1 , Y 2 , and Y 3 ), and the obtained data indicated that the quadratic model was well fitted ( Table 3). The selected formulation was further evaluated for drug release, permeation study, and cell line evaluation.

Particle Characterization
The PS, PDI, and ZP of the optimized LTN-CS-NLCs were observed to be 123.84 ± 3.72 nm, 0.13 ± 0.01, and +10.46 ± 1.84 mV, respectively (Figure 2A,B). While uncoated LTN-NLCs showed PS of 103.62 ± 5.76 nm, PDI of 0.11 ± 0.012, and ZP of −30.56 ± 4.32 mV, respectively. The small PS and PDI are one of the crucial properties for improved oral delivery. The low PDI value indicates a remarkable homogeneity of NPs. An insignificant increase in PS was noticed while developing LTN-CS-NLCs due to CS coating. Furthermore, CS coating leads to positive ZP from the negative ZP because of the cationic nature of CS ( Figure 2B). The coating of NPs with CS is a well-established technique to improve the oral delivery of drugs [35].

Surface Morphology
TEM also confirmed the surface morphology of LTN-CS-NLCs (Figure 3). The prepared delivery systems showed spherical shape particles with a smooth surface.

Particle Characterization
The PS, PDI, and ZP of the optimized LTN-CS-NLCs were observed to be 123.84 ± 3.72 nm, 0.13 ± 0.01, and +10.46 ± 1.84 mV, respectively (Figure 2A,B). While uncoated LTN-NLCs showed PS of 103.62 ± 5.76 nm, PDI of 0.11 ± 0.012, and ZP of −30.56 ± 4.32 mV, respectively. The small PS and PDI are one of the crucial properties for improved oral delivery. The low PDI value indicates a remarkable homogeneity of NPs. An insignificant increase in PS was noticed while developing LTN-CS-NLCs due to CS coating. Furthermore, CS coating leads to positive ZP from the negative ZP because of the cationic nature of CS ( Figure 2B). The coating of NPs with CS is a well-established technique to improve the oral delivery of drugs [35].

Surface Morphology
TEM also confirmed the surface morphology of LTN-CS-NLCs (Figure 3). The prepared delivery systems showed spherical shape particles with a smooth surface.

In Vitro Gastrointestinal Stability Study
The potential impact of SGF and SIF on the stability of LTN-CS-NLCs is depicted in Table 4 and Figure 4. Results of stability study of LTN-CS-NLCs in SIF demonstrated excellent stability with insignificant change in PS, PDI, and %EE. However, changes in PS, PDI, and %EE were observed in SGF after 12 h. In CS-NLCs, LTN could be continuously released or accumulated in the intestine region of gastrointestinal tract (GIT), which might lead to an increase in epithelial permeability, thereby promoting enhanced drug absorption [36].

In Vitro Gastrointestinal Stability Study
The potential impact of SGF and SIF on the stability of LTN-CS-NLCs is depicted in Table 4 and Figure 4. Results of stability study of LTN-CS-NLCs in SIF demonstrated excellent stability with insignificant change in PS, PDI, and %EE. However, changes in PS, PDI, and %EE were observed in SGF after 12 h. In CS-NLCs, LTN could be continuously released or accumulated in the intestine region of gastrointestinal tract (GIT), which might lead to an increase in epithelial permeability, thereby promoting enhanced drug absorption [36].

LTN Release Study
The release profiles of LTN from different formulations are depicted in Figure 5. LTN-CS-NLCs and LTN-NLCs revealed a biphasic release behavior. A rapid release in 2 h was found, after that a sustained LTN release up to 24 h was observed. The rapid LTN release in the initial 2 h could be due to the faster dissolution of LTN adsorbed on the NLCs surface [37]. The sustained release was due to the encapsulated LTN in the inner core of the lipid matrix that was released slowly by diffusion. Furthermore, LTN-CS-NLCs showed a much-delayed LTN release in comparison to the uncoated LTN-NLCs due to the CS coating. It protects the drug from desorption and diffusion [38]. The mechanism of LTN release was analyzed by fitting the data into the different release kinetic models. The Korsmeyer-Peppas model showed the highest correlation coefficient (R 2 = 0.9848). Therefore, the Korsmeyer-Peppas kinetic model was considered as the best-fitted model to explain the LTN release kinetics from LTN-CS-NLCs. Moreover, the exponent "n" of the release mechanism from the Korsmeyer-Peppas model was calculated, and the value was found to be 0.35, which stipulates Fickian diffusion mechanism from CS-NLCs.

LTN Release Study
The release profiles of LTN from different formulations are depicted in Figure 5. LTN-CS-NLCs and LTN-NLCs revealed a biphasic release behavior. A rapid release in 2 h was found, after that a sustained LTN release up to 24 h was observed. The rapid LTN release in the initial 2 h could be due to the faster dissolution of LTN adsorbed on the NLCs surface [37]. The sustained release was due to the encapsulated LTN in the inner core of the lipid matrix that was released slowly by diffusion. Furthermore, LTN-CS-NLCs showed a much-delayed LTN release in comparison to the uncoated LTN-NLCs due to the CS coating. It protects the drug from desorption and diffusion [38]. The mechanism of LTN release was analyzed by fitting the data into the different release kinetic models. The Korsmeyer-Peppas model showed the highest correlation coefficient (R 2 = 0.9848). Therefore, the Korsmeyer-Peppas kinetic model was considered as the best-fitted model to explain the LTN release kinetics from LTN-CS-NLCs. Moreover, the exponent "n" of the

Mucoadhesion Study
LTN-CS-NLCs revealed the higher mucoadhesive efficiency (70.46 ± 3.32%) compared to LTN-NLCs (22.58 ± 1.86%) and LTN suspension (14.67 ± 1.24%). The coating of NLCs with CS provided a significantly higher binding efficiency to mucin because of the electrostatic interactions between the positive charged CS and negatively charged mucin. Furthermore, hydrogen bonding as well as hydrophobic interactions between CS and mucin are also responsible for improved binding efficiency [39]. The higher mucoadhesive nature helps to achieve a longer residence time in GIT, therefore it will help to get the better therapeutic efficacy of the drug.

Mucoadhesion Study
LTN-CS-NLCs revealed the higher mucoadhesive efficiency (70.46 ± 3.32%) compared to LTN-NLCs (22.58 ± 1.86%) and LTN suspension (14.67 ± 1.24%). The coating of NLCs with CS provided a significantly higher binding efficiency to mucin because of the electrostatic interactions between the positive charged CS and negatively charged mucin. Furthermore, hydrogen bonding as well as hydrophobic interactions between CS and mucin are also responsible for improved binding efficiency [39]. The higher mucoadhesive nature helps to achieve a longer residence time in GIT, therefore it will help to get the better therapeutic efficacy of the drug.

Antioxidant Activity
DPPH is utilized to assess the antioxidant potential of a variety of drugs and drug delivery systems [27]. The DPPH changes color when it reacts with proton donor groups. Figure 6 represents the comparative antioxidant activity of LTN-CS-NLCs, LTN-NLCs, and pure LTN suspensions. The antioxidant potential of all the samples is directly dependent upon the LTN concentration. As the concentration of LTN increases, the antioxidant potential of LTN-CS-NLCs, LTN-NLCs, and pure LTN also statistically increases. LTN-CS-NLCs showed a maximum activity of 94.38 ± 5.34%, while LTN-NLCs and pure LTN depicted 76.24 ± 4.94% and 66.28 ± 4.28%, respectively. As per the observation, LTN-CS-NLCs represented statistically (p < 0.05) elevated antioxidant activity in comparison to both uncoated LTN-NLCs and pure LTN at all the tested concentrations. However, uncoated LTN-NLCs also showed excellent antioxidant activity compared to pure LTN. The higher antioxidant activity achieved by LTN-CS-NLCs and LTN-NLCs was due to the higher solubility of LTN in lipid present in the NLCs.

Antioxidant Activity
DPPH is utilized to assess the antioxidant potential of a variety of drugs and drug delivery systems [27]. The DPPH changes color when it reacts with proton donor groups. Figure 6 represents the comparative antioxidant activity of LTN-CS-NLCs, LTN-NLCs, and pure LTN suspensions. The antioxidant potential of all the samples is directly dependent upon the LTN concentration. As the concentration of LTN increases, the antioxidant potential of LTN-CS-NLCs, LTN-NLCs, and pure LTN also statistically increases. LTN-CS-NLCs showed a maximum activity of 94.38 ± 5.34%, while LTN-NLCs and pure LTN depicted 76.24 ± 4.94% and 66.28 ± 4.28%, respectively. As per the observation, LTN-CS-NLCs represented statistically (p < 0.05) elevated antioxidant activity in comparison to both uncoated LTN-NLCs and pure LTN at all the tested concentrations. However, uncoated LTN-NLCs also showed excellent antioxidant activity compared to pure LTN. The higher antioxidant activity achieved by LTN-CS-NLCs and LTN-NLCs was due to the higher solubility of LTN in lipid present in the NLCs.

Cytotoxicity Study
The potential outcomes of cytotoxicity study in MDA-MB-231 and MCF-7 cells are represented in Figure 7.

Cytotoxicity Study
The potential outcomes of cytotoxicity study in MDA-MB-231 and MCF-7 cells are represented in Figure 7.

Cytotoxicity Study
The potential outcomes of cytotoxicity study in MDA-MB-231 and MCF-7 cells are represented in Figure 7.

DAPI for Nuclear Staining
The toxic effect of LTN-CS-NLCs on MDA-MB-231 and MCF-7 cells was also examined by DAPI staining (Figure 8). DAPI is a nuclear stain that stains the unwound and damaged DNA in the nucleus. The exposure of cancer cells to LTN-NLCs and LTN-CS-NLCs resulted in significant changes in the morphology of the cell nucleus. It is clear from Figure 6 that the control cells stained negative with DAPI and the cells treated with LTN-NLCs and LTN-CS-NLCs emitted bright blue fluorescence which shows condensed and fragmented chromatin. In DAPI staining, the treated cells which are membrane-permeable selectively stain the nuclear material emitting fluorescence of apoptotic cells leaving the viable cells intact [41]. From the results obtained, it is can be concluded that LTN-CS-NLCs can serve as a potential candidate in the management of breast cancer. Figure 9A,B clearly revealed a significantly higher amount of LTN permeated and transported through the intestinal sac from optimized LTN-CS-NLCs and LTN-NLCs in comparison to LTN suspension. As per our findings, LTN-CS-NLCs exhibited about 1.5and 4.3-fold higher P app compared to LTN-NLCs and LTN suspension. The reason for the enhancement in P app was due to the presence of nonionic surfactant (P-188) in the NLCs as an excipient, which is a potent P-glycoprotein efflux pump inhibitor that was present on the mucous membrane of GIT. Furthermore, the mucoadhesive nature of LTN-CS-NLCs is also led to the disruption in the tight junctions of the gastrointestinal mucosa. The positive charge of CS-NLCs interacts with negatively charged gastrointestinal mucosa that helps to the opening of tight junctions. Therefore, a significantly higher quantity of drug permeated across the mucosa.

DAPI for Nuclear Staining
The toxic effect of LTN-CS-NLCs on MDA-MB-231 and MCF-7 cells was also examined by DAPI staining (Figure 8). DAPI is a nuclear stain that stains the unwound and damaged DNA in the nucleus. The exposure of cancer cells to LTN-NLCs and LTN-CS-NLCs resulted in significant changes in the morphology of the cell nucleus. It is clear from Figure 6 that the control cells stained negative with DAPI and the cells treated with LTN-NLCs and LTN-CS-NLCs emitted bright blue fluorescence which shows condensed and fragmented chromatin. In DAPI staining, the treated cells which are membrane-permeable selectively stain the nuclear material emitting fluorescence of apoptotic cells leaving the viable cells intact [41]. From the results obtained, it is can be concluded that LTN-CS-NLCs can serve as a potential candidate in the management of breast cancer.  Figure 9A,B clearly revealed a significantly higher amount of LTN permeated and transported through the intestinal sac from optimized LTN-CS-NLCs and LTN-NLCs in comparison to LTN suspension. As per our findings, LTN-CS-NLCs exhibited about 1.5and 4.3-fold higher P compared to LTN-NLCs and LTN suspension. The reason for the enhancement in P was due to the presence of nonionic surfactant (P-188) in the NLCs as an excipient, which is a potent P-glycoprotein efflux pump inhibitor that was present on the mucous membrane of GIT. Furthermore, the mucoadhesive nature of LTN-CS-NLCs is also led to the disruption in the tight junctions of the gastrointestinal mucosa. The positive charge of CS-NLCs interacts with negatively charged gastrointestinal mucosa that helps to the opening of tight junctions. Therefore, a significantly higher quantity of drug permeated across the mucosa.

Conclusions
In summary, LTN-CS-NLCs were prepared and optimized for improved LTN delivery and efficacy against breast cancer cells. The PS, PDI, and EE of the developed LTN-

Conclusions
In summary, LTN-CS-NLCs were prepared and optimized for improved LTN delivery and efficacy against breast cancer cells. The PS, PDI, and EE of the developed LTN-CS-NLCs were found to be satisfactory. LTN-CS-NLCs showed excellent gastrointestinal stability. TEM micrographs showed a spherical shape with a smooth surface. The CS coating provided modulation in LTN release from the NLCs and exhibited a sustained release profile for up to 24 h. There was significantly higher antioxidant activity found with LTN-CS-NLCs as compared to LTN-NLCs and pure LTN. LTN-CS-NLCs exhibited enhanced dose and time-dependent cytotoxicity in breast cancer cells compared to LTN-NLCs and pure LTN. Furthermore, LTN-CS-NLCs also depicted higher intestinal permeation compared to LTN-NLCs and pure LTN suspension. Therefore, our developed CS-NLCs of LTN represents excellent mucoadhesive nanoformulations to combat the challenges of LTN for improved delivery and therapeutic efficacy against breast cancer.