Influence of Various Drying Conditions on Phytochemical Compounds and Antioxidant Activity of Carrot Peel

(1) Background: Drying is an important process in the research of bioactive compounds. The aim of this study was to identify an optimal condition to dry carrot peel. (2) Methods: In this study, various drying conditions including hot-air (50 ◦C and 100 ◦C), vacuum (50 ◦C and 100 ◦C), microwave (600 W and 1200 W) and freeze dying (−45 ◦C) were applied, and the phytochemical yield and antioxidant activity of carrot peel were then assessed. (3) Results: The results showed that the highest amount of phytochemical compounds was achieved by microwave drying at 1200 W, followed by microwave drying at 600 W and freeze drying at −45 ◦C. In contrast, hot-air drying resulted in the lowest level of phytochemical compounds. Regarding the antioxidant activity of carrot peel, microwave drying at 1200 W was an optimal condition as it possessed the best antioxidant activity whereas hot-air, vacuum and freeze drying were not effective methods for retaining antioxidant activity. (4) Conclusions: Based on the results obtained from this study, microwave drying at 1200 W is recommended to dry carrot peel for potential application in the nutraceutical, beverage and/or functional food industries.

The biological oxidation process leads to the formation of active oxygen and free radicals species, resulting in oxidative stress-originated diseases, such as cardiovascular, diabetic and neurodegenerative diseases, and cancer [20,21].To prevent the radical chain reactions of oxidation or to inhibit the initiation and propagation step, leading to the termination of the reaction and delaying the oxidation process, natural antioxidants have been exploited and widely used [22].
Carrot is a popular root vegetable, which contains a significant amount of carotenoids, anthocyanidins and saponins [23,24].These compounds have been linked to the prevention of serious diseases by improving the immunology system.A major by-product obtained during the processing of carrot root is carrot peel, which is considered as a huge source of waste (approximately 5.28 million tonnes per year) [24] that increases the risk of pollution to the environment.Hence, there is potential to recycle carrot peel from the carrot processing industry as a rich source of bioactive compounds and pigments [25].
To date, there has been few reports on the optimal drying condition for the preparation of dried samples from carrot peel for further investigation and application.With this in mind, this study aimed to investigate the influence of various drying conditions on the phytochemical compounds and antioxidant activity of carrot peel for potential application in the nutraceutical, beverage and/or functional food industries.

Materials and Chemicals
Ten kg of carrot roots (Scarlet Nantes) were purchased from a post-harvest market in Westfield, Tuggerah, Central Coast, New South Wales, Australia (March 2016) and immediately transported to the laboratories at the University of Newcastle, Ourimbah Campus, New South Wales, Australia.Carrot peel was then separated from carrot root using a manual peeler and stored at −20 • C in the freezer until required for further investigation.

Preparation of Dried Carrot Peel
Fresh carrot peel was dried to a constant weight at various drying conditions based on the previously described methods in [6,15] with some modifications as follows.
Firstly, 50 g of fresh sample was weighed before drying for each experiment.Hot-air Drying: Drying was performed in a hot-air oven (Anax Pty Ltd., Sydney, Australia) at 50 • C (HAD50) and 100 • C (HAD100).
Microwave Drying: Fresh samples were placed in the middle of a microwave oven (Sharp Carousel, Sharp Corporation, Bangkok, Thailand) and dried at power levels of 600 W (MWD600) and 1200 W (MWD1200).
Freeze Drying: Drying was conducted in a freeze drier (Rietschle Thomas Australia Pty Ltd., Seven Hills, NSW, Australia) at −45 • C and 83 kPa.
After drying, the samples were reweighed to determine their drying yield as shown in Equation (1) [15]: Here, DY (g dried sample/100 g fresh sample) is drying yield, DS (g) is the weight of the dried sample after drying, and FS (g) is the weight of the fresh sample before drying.
The drying time was recorded for each experiment using a timer.The energy consumption of the various drying methods were estimated in Equation ( 2) [26] as follows: Here, W i is the consumed electrical energy of the drying method (i) (kWh), Pi is the electrical power supplied in the drying method (i) (kW), and t i is the time taken for the drying method (i) (h).
The initial moisture of the fresh sample and the residual moisture of dried samples following drying were determined according to the AOAC official methods of analysis [27] using the hot-air drying method at 100 • C overnight.The dried samples were then ground to a fine powder using an electric blender (Hamilton Beach Brands, Inc., Shenzhen, China), screened through a stainless-steel mesh with a particle size of ≤1.4 mm (Endecotts, London, UK), then packed in the sealed polyamide bags, and stored at −20 • C in the freezer until used for further investigation.

Preparation of Methanol Extract from Dried Carrot Peel
The methanol extracts of the dried carrot peel were prepared based on the previously reported method in [15,24].0.2 g of dried sample was extracted with 20 mL of methanol at room temperature (20 ± 1 • C) for 30 min, then the microwave-assisted extraction method was applied for 60 min using a microwave oven (Sharp Carousel; Sharp Corporation, Bangkok, Thailand) at power of 360 W and the irradiation time was 5 s per 2 min period (total irradiation time of 150 s).
After extraction, carrot peel extracts were immediately cooled down to room temperature using an ice water bath and then filtered to obtain the extracts for analysis of their bioactive compounds and antioxidant activity.To determine the extraction yield, 2 mL of extract was dried in a hot-air oven (Anax Pty Ltd., Sydney, Australia) at 90 • C for 4 h to a constant weight.The extraction yield is shown in Equation (3) [15]: Here, EY (g dried extract/100 g dried sample) is the extraction yield, DE (g) is the weight of the dried extract after extraction, and DS (g) is the weight of the dried sample before extraction.

Total Phenolic Content (TPC)
The TPC of carrot peel extracts was determined using the Folin-Ciocalteu reagent based on the previously described method in [15,28].0.5 mL of the extract was thoroughly mixed with 2.5 mL of 10% (v/v) Folin-Ciocalteu reagent in distilled water.The mixture was kept for 6 min, then 2 mL of 7.5% (w/v) Na 2 CO 3 solution was added to the mixture and incubated for 1 h in the dark at room temperature.The absorbance of the mixture was measured at 765 nm using a UV-VIS spectrophotometer (Cary 50 Bio, Mulgrave, VIC, Australia).Methanol and gallic acid were used as a control and standard.TPC was expressed as mg of gallic acid equivalents (GAE)/g dried sample.

Total Flavonoid Content (TFC)
The TFC of carrot peel extracts was estimated using the formerly established method in [15,28].0.5 mL of extract was thoroughly mixed with 2 mL of distilled water and 0.15 mL of 5% (w/v) NaNO 2 solution and left for 6 min.0.15 mL of 10% (w/v) AlCl 3 solution was then added and kept for a further 6 min.Finally, 2 mL of 4% (w/v) NaOH solution and 0.7 mL of distilled water were added and incubated for 15 min in the dark at room temperature.The absorbance of the mixture was measured at 510 nm using a UV-VIS spectrophotometer.Methanol and rutin were used as a control and standard, respectively.TFC was expressed as mg of rutin equivalents (RE)/g dried sample.

Proanthocyanidin Content (PC)
The PC of carrot peel extracts was determined using the previously described method in [15,28].0.5 mL of extract was thoroughly mixed with 3 mL of 4% (w/v) vanillin solution, then 1.5 mL of concentrated HCl (37% w/v) was added and the mixture was incubated for 15 min in the dark at room temperature.The absorbance of the mixture was measured at 500 nm using a UV-VIS spectrophotometer.Methanol and catechin were used as a control and standard, respectively.PC was expressed as mg of catechin equivalents (CE)/g dried sample.

Saponin Content (SC)
The SC of carrot peel extracts was determined according to the formerly described method in [15,28].0.5 mL of the extract was thoroughly mixed with 0.5 mL of 8% (w/v) vanillin solution, then 5 mL of 72% (v/v) H 2 SO 4 solution was added to the mixture, incubated at 70 • C for 10 min in the dark at room temperature and rapidly cooled in an ice water bath to room temperature.The absorbance of the mixture was measured at 560 nm using a UV-VIS spectrophotometer.Methanol and escin were used as a control and standard, respectively.SC was expressed as mg of escin equivalents (EE)/g dried sample.

ABTS Radical Scavenging Capacity (ARSC)
The ARSC of carrot peel extracts was determined using the ABTS assay according to the previously described method in [15,28].A stock solution was prepared by mixing 7.4 mM ABTS •+ (2,2 -Azino-bis-3-ethylbenzothiazoline-6-sulphonic acid) and 2.6 mM K 2 S 2 O 8 solutions (1:1 ratio) and then incubating for 12 h in the dark at room temperature; then, they were stored at −18 • C until required.Before the ABTS reaction, a working solution was prepared by mixing 1 mL of stock solution with 60 mL of methanol to obtain an absorbance of 1.1 ± 0.02 at 734 nm.After that, 0.15 mL of the extract was thoroughly mixed with 2.85 mL of the working solution and incubated for 2 h in the dark at room temperature.The absorbance of the mixture was measured at 734 nm using a UV-VIS spectrophotometer.Methanol and trolox were used as a control and standard, respectively.The results were expressed as mg trolox equivalents (TE)/g dried sample.

DPPH Radical Scavenging Capacity (DRSC)
The DRSC of carrot peel extracts was measured based on the formerly reported method in [15,28].A stock solution of 0.024% (w/v) DPPH (2,2-diphenyl-1-picryl-hydrazil) in methanol was prepared and stored at −18 • C until required.Prior to the DPPH reaction, a working solution was prepared by diluting 1.0 mL of stock solution with 45 mL of methanol to obtain an absorbance of 1.1 ± 0.02 at 515 nm.Next, 0.15 mL of the extract was thoroughly mixed with 2.85 mL of the working solution and incubated for 3 h in the dark at room temperature.The absorbance of the mixture was measured at 515 nm using a UV-VIS spectrophotometer.Methanol and trolox were used as a control and standard, respectively.The results were expressed as mg trolox equivalents (TE)/g dried sample.

Cupric Ion Reducing Antioxidant Capacity (CUPRAC)
The CUPRAC of carrot peel extracts was analyzed using the previously described method in [15,28].Before the CUPRAC reaction, 1.0 mL of 10 mM CuCl 2 solution was thoroughly mixed with 1.0 mL of 7.5 mM neocuproine and 1.0 mL of 7.7% (w/v) NH 4 Ac solutions.After that, 1.1 mL of the extract was added to the mixture and incubated for 1.5 h in the dark at room temperature.The absorbance of the mixture was measured at 450 nm using a UV-VIS spectrophotometer.Methanol and trolox were used as a control and standard, respectively.The results were expressed as mg trolox equivalents (TE)/g dried sample.

Ferric Reducing Antioxidant Power (FRAP)
The FRAP of carrot peel extracts was determined according to the formerly reported method in [15,28].Firstly, three reagents were prepared including Reagent A: 300 mM acetate buffer solution, pH 3.6; Reagent B: 10 mM TPTZ (2,4,6-tripyridyl-s-triazine) solution in 40 mM HCl; and Reagent C: 20 mM FeCl 3 •6H 2 O solution.Prior to the FRAP reaction, the fresh FRAP solution was prepared by mixing reagents A, B and C at a ratio of 10:1:1.Next, 0.15 mL of the extract was thoroughly mixed with 2.85 mL of the fresh FRAP solution and incubated for 30 min in the dark at room temperature.The absorbance of the mixture was read at 593 nm using a UV-VIS spectrophotometer.Methanol and trolox were used as a control and standard, respectively.The results expressed as mg trolox equivalents (TE)/g dried sample.

Statistical Analysis
All experiments were carried out in triplicate.The data were analyzed using SAS software (Version 9.2, SAS Inst., Inc., Cary, NC, USA) and expressed as mean ± standard deviation (n = 3).One-way analysis of variance (ANOVA) and Tukey HSD tests were used for statistical comparisons.Significant differences were considered when p-values were less than 0.05 (p < 0.05).

Effect of Drying Conditions on Physicochemical Properties of Carrot Peel
Table 1 describes the drying time, drying yield, residual moisture, extraction yield and energy consumption of carrot peel using various drying methods and conditions.Among them, the drying time was strongly affected by temperature and widely varied between four drying methods (from 0.08 to 70 h).Freeze drying took 70 h to dry carrot peel at the lowest temperature (−45 • C), while microwave drying at 1200 W took only 0.08 h.The drying time in this study was longer than that in the research of Nguyen et al. [6] on the P. amarus when using six drying methods including thermal and non-thermal drying (from 0.15 to 23.75 h).The drying yield was increased with an increase in the drying temperature.
The highest drying yield was obtained by using vacuum drying at 100 • C (12.75 g dried sample/100 g fresh sample), which was significantly different from the other drying conditions, excepted for hot-air drying at 100 • C. The authors [6] indicated that the drying yield obtained from P. amarus was up to 23.84 g dried sample/100 g fresh sample.In regards to residual moisture, vacuum drying of carrot peel at 100 • C resulted in the lowest residual moisture in the product (3.13 g water/100 g dried sample), while freeze drying, vacuum drying at 50 • C, and hot-air drying at 50 • C were the least effective methods because of higher residual moisture (6.91, 7.0 and 6.86 g water/100 g dried sample, respectively).As a result, extraction yield obtained by vacuum drying at 100 • C was the highest (44.8 g dried extract/100 g dried sample), followed by vacuum drying at 50 • C and microwave drying at 600 W, whereas microwave drying at 1200 W resulted in the lowest extraction yield (27.6 g dried extract/100 g dried sample).In comparison with other materials, the extraction yield of sea grape and P. amarus by hot-air drying was only 7.62 and 13.17 g dried extract/100 g dried sample, respectively [6,29].Regarding energy consumption, freeze drying might seem to be the most expensive method because it uses the largest amount of energy (245 KWh), whereas microwave drying consumed the least energy due to the use of microwave radiation.Overall, the different drying conditions led to the differences in the drying time, drying yield, extraction yield and residual moisture of carrot peel as well as their energy consumption.Of these, microwave drying at 1200 W was the fastest and cheapest method for preparation of dried carrot peel for further investigation and application.

Total Phenolic Content (TPC)
Table 2 indicates that the TPC of carrot peel was different for different drying conditions.Of these, TPC prepared by microwave drying at 1200 W (23.49 mg GAE/g dried sample) was significantly higher (p < 0.05) than those obtained from other drying conditions, while hot-air drying resulted in the lowest amount of TPC.An increase in the temperature in thermal drying methods caused a decrease in TPC (4.8 and 2.74 mg GAE/g dried sample at HAD50 and HAD100, respectively) or (3.77 and 3.11 mg GAE/g dried sample at VCD50 and VCD100, respectively).Interestingly, TPC in microwave drying at 1200 W was significantly higher than that at 600 W. The reason for these differences may be due to different drying conditions, particularly drying temperature and time.The same figure has been reported by Nguyen et al. [6], who indicated that the TPC of P. amarus was greatly affected by drying time and temperature.Other studies [14][15][16] have also indicated that microwave drying can maintain high TPC of P. trimera root, Vitex negundo tea and banana peel.However, Lim et al. [12] found that microwave drying resulted in reducing a great amount of the TPC from the P. amarus.

Total Flavonoid Content (TFC)
Table 2 illustrates the TFC of carrot peel achieved by four different drying methods.In general, TFC increased with a rise in drying temperature.Microwave drying at 1200 W (MWD1200) possessed the highest amount of TFC (28.09 mg RE/g dried sample), followed by MWD600 (20.29 mg RE/g dried sample) whereas the lowest TFC was obtained from hot-air drying, regardless of drying temperature.The reason for these results may be due to the faster drying time in MWD1200 (0.08 h) as compared to HAD50 (25 h).This finding is different from the results of Nguyen et al. [6], who indicated that the TFC of P. amarus dramatically decreased in microwave drying.On the other hand, other reports [15,16] showed that the higher TFC of P. trimera root and banana peel was obtained by microwave drying as compared to vacuum and hot-air drying methods.

Proanthocyanidin Content (PC)
The PC of carrot peel increased in the order of the drying methods as follows: hot-air drying > vacuum drying > freeze drying > microwave drying (Table 2).Carrot peel that was dried by microwave had the highest level of proanthocyanidins (6.89 and 4.59 mg CE/g dried sample at 1200 W and 600 W, respectively), which was significantly higher (p < 0.05) than that obtained from other drying conditions.Using hot-air to dry carrot peel significantly decreased (p < 0.05) the amount of proanthocyanidins (1.88 mg CE/g dried sample) as compared to that obtained by freeze drying (2.67 mg CE/g dried sample).Freeze drying and vacuum drying showed no significant difference in the content of proanthocyanidins (2.67 and 2.37 mg CE/g dried sample, respectively).This result is different from the studies of the authors in [6,15] on the P. amarus and P. trimera root, which showed that PC in hot-air drying was significantly higher (p < 0.05) than in microwave and vacuum drying.The data obtained from this study indicated that drying methods and drying time greatly affected the PC of carrot peel.Among the different drying methods and conditions tested, microwave drying seemed to be the most effective method for maintaining high PC from carrot peel.

Saponin Content (SC)
Table 2 shows that SC was maintained at the highest level in the carrot peel when it was dried by microwave at 1200 W (353.87 mg EE/g dried sample), followed by MWD600, freeze drying and vacuum drying at 50 • C (291.23, 283.58 and 262.11 mg EE/g dried sample, respectively).Hot-air drying resulted in the lowest amount of saponins (213.03mg EE/g dried sample).The SC of carrot peel was higher than that of the P. amarus, which ranged from 121.18 to 250.34 mg EE/g dried sample [6].The highest SC of the P. amarus was obtained by infrared drying [6] whereas low-pressure superheated steam drying at 50 • C achieved higher total triterpene saponin content from C. asiatica leaves than those obtained by combined infrared-hot air drying and hot-air drying [1].Consequently, SC differs from species to species and is greatly affected by the drying method, and carrot peel is a rich source of saponins as compared to other plants like the P. amarus.Saponins have been shown to possess various biological effects, such as antiviral, antimicrobial, antioxidative, immunomodulatory, antiherbivore, anti-hyperglycaemic, hepatoprotective, cardioprotective, anti-HIV, cytotoxic, antitumor, anticancer, anti-inflammatory, and antihepatitis B and C activities [28,30,31].Therefore, carrot peel is a promising source for the extraction of saponins for potential application in nutraceuticals and/or functional foods.

Phytochemical Compounds in the Dried Carrot Peel
Figure 1 shows the representative HPLC chromatogram of methanol extract from the carrot peel prepared by microwave drying at 1200 W. Based on retention time, gallic acid was firstly identified, followed by rutin, p-coumaric acid, (±)-naringenin, protocatechuic acid, and apigenin (3.59, 3.93, 28.26, 32.73, 34.82, and 44.21 min, respectively).Some of the major phytochemicals in the carrot peel extract need to be identified in further studies.Gallic acid was also the first phytochemical in the extracts from the P. amarus and P. trimera root to be detected by HPLC [6,15].

Phytochemical Compounds in the Dried Carrot Peel
Figure 1 shows the representative HPLC chromatogram of methanol extract from the carrot peel prepared by microwave drying at 1200 W. Based on retention time, gallic acid was firstly identified, followed by rutin, p-coumaric acid, (±)-naringenin, protocatechuic acid, and apigenin (3.59, 3.93, 28.26, 32.73, 34.82, and 44.21 min, respectively).Some of the major phytochemicals in the carrot peel extract need to be identified in further studies.Gallic acid was also the first phytochemical in the extracts from the P. amarus and P. trimera root to be detected by HPLC [6,15].

ABTS Radical Scavenging Capacity (ARSC)
Table 3 shows that the ARSC of carrot peel varied depending on the drying method.The highest ARSC was achieved by microwave drying at 1200 W (166.35 mg TE/g dried sample), which was significantly higher (p < 0.05) than that dried by MWD600 and FD (85.70 and 23.81 mg TE/g dried sample, respectively).In contrast, hot-air and vacuum drying seemed to destroy all the ARSC of carrot peel.The same finding was reported by Vu et al. [16], who indicated that microwave drying at 1200 W maintained the greatest ARSC of banana peel as compared to other drying methods.The ARSC of carrot peel in this study is lower than that in the P. amarus using six different drying methods, which ranged from 384.86 to 860.16 mg TE/g dried sample [6].Strong correlations were found between the ARSC and phytochemicals of carrot peel, especially TPC, TFC and proanthocyanidins (R 2 = 0.99, 0.95 and 0.98, respectively; Table 4).This reveals that TPC, TFC and proanthocyanidins are key components for the ARSC of carrot peel.

DPPH Radical Scavenging Capacity (DRSC)
Table 3 shows that microwave drying was the most effective method for removing moisture from carrot peel because of its high DRSC retention, whereas vacuum drying had a negative influence  Table 3 shows that the ARSC of carrot peel varied depending on the drying method.The highest ARSC was achieved by microwave drying at 1200 W (166.35 mg TE/g dried sample), which was significantly higher (p < 0.05) than that dried by MWD600 and FD (85.70 and 23.81 mg TE/g dried sample, respectively).In contrast, hot-air and vacuum drying seemed to destroy all the ARSC of carrot peel.The same finding was reported by Vu et al. [16], who indicated that microwave drying at 1200 W maintained the greatest ARSC of banana peel as compared to other drying methods.The ARSC of carrot peel in this study is lower than that in the P. amarus using six different drying methods, which ranged from 384.86 to 860.16 mg TE/g dried sample [6].Strong correlations were found between the ARSC and phytochemicals of carrot peel, especially TPC, TFC and proanthocyanidins (R 2 = 0.99, 0.95 and 0.98, respectively; Table 4).This reveals that TPC, TFC and proanthocyanidins are key components for the ARSC of carrot peel.

DPPH Radical Scavenging Capacity (DRSC)
Table 3 shows that microwave drying was the most effective method for removing moisture from carrot peel because of its high DRSC retention, whereas vacuum drying had a negative influence on the DRSC.The highest ARSC was seen in microwave drying at 1200 W (97.41 mg TE/g dried sample) which differed significantly from other drying conditions.Microwave drying at 600 W resulted in a significantly lower ARSC (48.33 mg TE/g dried sample), followed by freeze drying (23.74 mg TE/g dried sample), and hot-air drying at 50 • C (17.99 mg TE/g dried sample).However, the DRSC of carrot peel was completely lost when using hot-air drying at 100 • C. Table 4 shows the correlation between the phytochemical compounds and antioxidant activity of carrot peel dried by different methods.The DRSC and TPC, TFC and proanthocyanidins had strong correlations (R 2 = 0.98, 0.92 and 0.93, respectively), while a moderate correlation was observed for the DRSC and saponins (R 2 = 0.79).This indicates that TPC, TFC and proanthocyanidins are major contributors to the DRSC of carrot peel.This outcome is supported by previous studies [16,32], which found that microwave drying of banana peel and sage plants resulted in the highest DRSC, whereas the lower DRSC was associated with hot-air and vacuum drying methods.However, the result obtained in this study is different from the findings of Nguyen et al. [6], who indicated that the DRSC of the P. amarus was only significantly affected by low-temperature-air drying, microwave drying at all power levels, and sun drying.

Cupric Ion Reducing Antioxidant Capacity (CUPRAC)
The same trend is observed for the CUPRAC of carrot peel (Table 3), in which microwave drying at 1200 W possessed the highest CUPRAC (24.03 mg TE/g dried sample), and it was significantly higher (p < 0.05) than other drying conditions.Freeze drying retained a limited CUPRAC of 6.48 mg TE/g dried sample, which was not significantly different from hot-air drying at 50 • C (4.73 mg TE/g dried sample).In contrast, vacuum drying achieved the lowest CUPRAC (2.36-2.87mg TE/g dried sample).This result is similar to the outcome of Vu et al. [16], who showed that the highest CUPRAC of banana peel was obtained by microwave drying at 960 W (65 mg TE/g dried sample).Table 4 illustrates that there were strong correlations between TPC, TFC and proanthocyanidins and the CUPRAC of carrot peel (R 2 = 1.00, 0.92 and 0.96, respectively), while a weaker correlation was found between saponins of carrot peel and its CUPRAC (R 2 = 0.82).This reveals that TPC, TFC and proanthocyanidins are the main contributors for the CUPRAC of carrot peel.

Ferric Reducing Antioxidant Power (FRAP)
Table 3 indicates that the FRAP of carrot peel varied in a range from 9.56 to 95.19 mg TE/g dried sample.In general, the FRAP was decreased in order of microwave, freeze, hot-air and vacuum drying.Again, the highest FRAP was obtained from microwave drying at 1200 W, which was twice as high as that dried at 600 W (95.19 and 48.07 TE/g dried sample, respectively) and both were significantly different (p < 0.05) from other drying conditions.Freeze drying also possessed more than one fourth the FRAP of MWD1200 (21.67 TE/g dried sample).The strongest correlation was observed for the FRAP and TPC of carrot peel, followed by proanthocyanidins, TFC and saponins (R 2 = 1.00, 0.98, 0.90 and 0.81, respectively; Table 4), implying that TPC, proanthocyanidins and TFC are key contributors for the FRAP of carrot peel.This finding is similar to the report of Vu et al. [16], who indicated that the FRAP of banana peel was achieved at the highest level by microwave drying, followed by freeze drying, vacuum drying, hot-air drying, dehumidified air drying, and sun drying methods.

Conclusions
This study indicated that different drying methods and conditions greatly influenced the amount of certain bioactive compounds and the antioxidant activity of carrot peel.Among the different drying methods used, microwave drying was the most effective method to dry carrot peel, while hot-air, vacuum and freeze drying were less effective methods.Microwave drying at 1200 W achieved the highest level of phytochemical compounds, while hot-air drying obtained the lowest content of bioactive compounds.Additionally, the antioxidant activity was also maximized when carrot peel was dried by microwave at 1200 W, but it was significantly reduced in hot-air, vacuum and freeze drying methods.

Figure 1 .
Figure 1.HPLC chromatogram of methanol extract from the carrot peel prepared by microwave drying at 1200 W, with UV-VIS detector set at 340 nm.

Figure 1 .
Figure 1.HPLC chromatogram of methanol extract from the carrot peel prepared by microwave drying at 1200 W, with UV-VIS detector set at 340 nm.

Table 1 .
Physicochemical properties of carrot peel dried at various conditions (n = 3).

Table 3 .
Antioxidant activity of carrot peel dried at various conditions (n = 3).

Table 4 .
Correlations between phytochemical compounds and antioxidant activity of carrot peel dried at various conditions.