69 ThapaB HPLCanalysis-Capsaicin JMedFood 2009 PDF
69 ThapaB HPLCanalysis-Capsaicin JMedFood 2009 PDF
69 ThapaB HPLCanalysis-Capsaicin JMedFood 2009 PDF
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ABSTRACT Capsicum fruit, a popular spice as chili pepper, is an important ingredient of the formulations used in
traditional medicines. Moreover, Capsicum fruit is listed as an official drug in several pharmacopoeias. Capsaicin, the most
abundant component in Capsicum fruit, exhibits its therapeutic and adverse effects in a dose-dependent manner. Therefore, the
known capsaicin content is the prerequisite for optimizing any formulation based on Capsicum fruit as a crude drug. We
studied 16 samples of Capsicum fruits grown at different altitudes in Nepal and determined their capsaicin content by high-
performance liquid chromatography. The capsaicin content was found to range from 2.19 to 19.73 mg=g of dry weight of
Capsicum fruits. Capsaicin content in pericarp was found to be higher than in seeds. No correlation was found between the
shape or size of the fruits and its capsaicin content. Our findings indicate that many of the formulations prepared from
Capsicum fruit, even as described in pharmacopoeias, may vary in their strength, therapeutic activity, and possible side effects
if the capsaicin content in Capsicum fruit is not standardized.
KEY WORDS: capsaicin Capsicum fruits Capsicum tincture high-performance liquid chromatography pain
Solanaceae
908
HPLC ANALYSIS OF CAPSICUM FRUITS 909
Table 1. Capsaicin Content of Varieties of Capsicum Fruits Collected from Different Places in Nepal
Sample (voucher Capsaicin
number) Latin name Local name Place (date of collection) content (mg=g)a
A (312) C. annum Lwang Khursani Chitwan ( July 11, 2004) 10.27 1.06
B (313) C. annum Marchai Sukrabare Hatbazar, Biratnagar 3.60 0.71
(October 29, 2004)
C (314) C. annum Jire Khursani Tharpu, Tanahun (August 25, 2004) 8.91 0.39
(var. glabourculum)
D (315) C. annum Suryamukhi Malepatan, Pokhara ( June 24, 2004) 5.21 0.35
(var. Suryamukhi) Khursani
E (316) C. frutescens Dalle Khursani Parsevati, Syanja (October 10, 2004) 11.71 1.13
F (317) C. annum Khursani Gorkha ( July 25, 2004) 4.77 0.38
G (318) C. annum Chilli Silugudi (bought from Pokhara) 4.97 0.21
( June 20, 2004)
H (319) C. annum Khursani Methavurung, Syanja ( July 12, 2004) 6.01 0.83
I (320) C. annum Jire Khursani Bagmara, Kaski (October 15, 2004) 6.88 0.24
(var. glabourculum)
J (321) C. annum Khursani Khairenitar, Tanahun ( July 11, 2004) 4.54 0.86
K (322) C. frutescens Jyanmara Khursani Dakshinkali, Kathmandu ( July 11, 2004) 3.14 0.45
L (323) C. annum Nangi Marchai Rani, Biratnagar (October 25, 2004) 8.14 0.45
M (324) C. annum Khursani Jiling, Trishuli (October 07, 2004) 2.83 0.10
N (325) C. annum Khursani Bagmara, Kaski (October 20, 2004) 2.19 0.22
O (326) C. annum Nepali Khursani Lubu, Lalitpur (December 05, 2004) 2.24 0.11
P (327) C. annum Khursani Pidikhola, Syanja (August 12, 2004) 19.73 1.61
E (316)b C. frutescens Dalle Khurseni Parsevati, Syanja 4.34 0.01
K (322)b C. frutescens Jyanmara Khursani Dakshinkali, Kathmandu 0.98 0.13
M (324)b C. annum Khursani Jiling, Trishuli 0.53 0.24
O (326)b C. annum Nepali Khursani Lubu, Lalitpur 0.63 0.13
a
The quantity of capsaicin (mg) in Capsicum fruit (g of dry weight) was expressed as mean standard deviation (n ¼ 3). The data were obtained by calculating the
HPLC peak area with the correlation equation (y ¼ 242,906x 11,177) and correlation coefficient (R2 ¼ 0.999).
b
Dried seeds of these samples were used for the determination of capsaicin content.
Nepal in order to utilize them as therapeutic agents with methanol used were of high-performance liquid chroma-
minimal side effects. Determination of the capsaicin content tography (HPLC) grade. Double distilled water was used
in each Capsicum fruit is needed to predict the potency and throughout the experiment, and all other solvents and other
efficacy of topical Capsicum tincture and oral Capsicum chemicals used were of analytical grade.
powder, enabling the optimization of therapeutic outcome
and control over its side effects. Apparatus
The HPLC system consisted of Shimadzu (Kyoto, Japan)
MATERIALS AND METHODS HPLC pump LC-9A, Shimadzu 6PD-6A ultraviolet spec-
Plant materials trophotometer detector, and Shimadzu C-R5A Chromatopac
data processor. The column was RP18 Fluofix 3NW415
The mature Capsicum fruits were harvested from differ- (4.6150 mm) joined with a precolumn.
ent places in Nepal (Table 1), and photographs of Capsicum
fruits are presented in Figure 1. All fruits were dried in the
Preparation of standard solutions
shade. The dried fruits were freed from seeds, ground, and
stored in air-tight containers in the refrigerator until exam- A stock solution of capsaicin was made by dissolving
ination. Capsicum fruits were identified by comparing au- 2 mg of standard capsaicin in 2 mL of methanol. Working
thentic samples and also confirmed with the help of an solutions were prepared by diluting the stock solution to the
expert. The voucher sample of each material is recorded as desired concentration with methanol.
a specified voucher number in Table 1 and preserved in
the Museum of Natural Medicine, The School of Pharma- Chromatographic conditions
ceutical and Biomedical Sciences, Pokhara University,
Pokhara, Nepal. The mobile phase consisted of 0.1% phosphoric acid=
acetonitrile (3:2 vol=vol). The temperature of the column
was maintained at 308C during the chromatographic sepa-
Reagents and materials
ration. The flow rate was 0.8 mL=minute, and the chroma-
Standard capsaicin (purity 99%) was obtained from Wako tography was run for 25 minutes. The eluting compounds
Pure Chemical Industries (Osaka, Japan). Acetonitrile and were monitored at a wavelength of 281 nm.
910 THAPA ET AL.
Extraction and capsaicin content determination volume was adjusted to 25 mL by addition of methanol. The
samples were centrifuged and passed through a Millipore
Each powder sample was put in a Petri dish and kept in (Billerica, MA) nylon filter (pore size, 0.45 mm). The sam-
the oven at 608C for 1 hour to make it dry. One gram of each ples were packed in the vials and kept in the refrigerator
powder sample was transferred into the volumetric flask until examination. Extraction of seeds of some Capsicum
(25 mL) and filled with methanol. Volumetric flasks were fruits was also performed in the same way as described
kept in the water bath at 508C for 4 hours, and the entire above. The sample solution or standard capsaicin solution
contents were left overnight at room temperature. The final (20 mL) was directly injected into the HPLC apparatus.
HPLC ANALYSIS OF CAPSICUM FRUITS 911
RESULTS
Calibration
The determination of capsaicin in Capsicum fruit extract
was performed using the external standard method. The
calibration graphs were expressed as chromatographic peak
areas of standard capsaicin versus corresponding concen-
trations of the standard in the concentration range of 50–
1,000 mg=mL.
been considered to be inversely proportional to the size of the limited knowledge on its minor constituents, and the
the fruit.18 However, our experiment showed capsaicin differences in potency between natural capsaicinoids require
content in Capsicum fruit not to be related to the size of the standardization of Capsicum fruits prior to manufacturing of
fruit. The fruit with the highest capsaicin content was among drug formulations. In addition, determination of capsaicin
the largest fruits (19.73 mg=g), whereas the smallest Cap- content in Capsicum fruits enables us to recommend a daily
sicum fruit had the third highest capsaicin content (10.27 dose as a food additive, which would be a very cheap and
mg=g) (Fig. 1). available preventive nutrient in gastrointestinal disorders.
In Nepal, chili is generally harvested from the beginning
of autumn to late autumn. Harvesting time widely varies ACKNOWLEDGMENTS
because of the type of chili cultivated by the farmers and
climate variation due to the sharp altitude variation. In this The authors are indebted to Prof. Dr. Radheshyam
study, we are unable to correlate the level of pungency with Kayastha, Tribhuvan University, Nepal for his help in
regard to the time of harvesting. identification of some samples. This work was partially
Capsicum frutescens is generally considered as a hotter supported by a Pokhara University research grant, for which
chili in Nepal. In this study, samples E and K were identified the authors express their gratitude.
as C. frutescens because of their morphologically similari-
ties and plant identification; however, their capsaicin con- AUTHOR DISCLOSURE STATEMENT
tents differed by almost 400%. Similarly, the capsaicin No competing financial interests exist.
content among Capsicum annum was found to vary from
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