Volume : 10, Issue : 05, May – 2023

Title:

30.DEVELOPMENT AND VALIDATION OF HERBAL DRUG-LOADED TOPICAL NIOSOMAL GEL FOR TREATMENT OF ECZEMA

Authors :

Akash C. Garudkar*, Dr.Monika Jadhao, Diksha D. Ghorpade

Abstract :

To create and validate a straightforward, accurate, and affordable UV-visible spectrophotometric method for calculating Calendulla officinalis and nelumbo nucifera in accordance with ICH Q2 (R1) guidelines. A UV-spectrophotometric technique has been devised for the simultaneous quantification of calendulla officinalis and nelumbo nucifera in a formulation of niosomal gel for the treatment of dermatitis. The stock solution is made using methanol as a solvent, and subsequent dilutions are made in distilled water. Calendula officinalis and nelumbo nucifera calibration standards were created, and absorbance was measured at the wavelength of maximum absorption. The linearity and range of the calibration curve of concentration vs. absorbance were computed. Additionally, it demonstrates that nelumbo nucifera and Calendulla officinalis both display absorption maxima at 320 nm and 254 nm, respectively. In the concentration ranges of 2–10 g/ml for Calendulla officinalis and 10–50 g/ml for nelumbo nucifera, respectively, the system followed Beer’s law. According to ICH standards, the method was verified for linearity, range, accuracy, precision, and recovery studies. The routine examination of Calendulla officinalis and nelumbo nucifera in the formation of niosomal gel was therefore found to benefit from the suggested method’s rapidity, specificity, precision, accuracy, and cost-effectiveness as a quality control tool. A simple, precise and cost-effective UV- visible spectrometry method for the estimation of niosomal gel was developed. The said method was developed using economical percentage of organic phase in aqueous media as solvent. Said validated UV- visible method can be efficiently used for the estimation of Calendulla officinalis and nelumbo nucifera in bulk as well as formulation.
Keywords: UV- visible spectrometry, Calendulla officinalis, Nelumbo nucifera, validation

Cite This Article:

Please cite this article in press Akash C. Garudkar et al,. Development and Validation Of Herbal Drug-loaded Topical Niosomal Gel for Treatment Of Eczema., Indo Am. J. P. Sci, 2023; 10 (05).

Number of Downloads : 10

References:

1. Kasper, Braun W, Fauci, Hauser, Longo, Jameson. Harrison’s Principles of Internal Medicine, 16th ed, USA, 2004, 1132.
2. Skoog, Holler, Nieman. Principles of Instrumental Analysis, fifth edition, Thomson Asia Pvt. Ltd., Singapore, 2004, 300-325.
3. Beckett A, H Stenlake. Practical Pharmaceutical Chemistry, 4th edition, CBS Publishers and Distributors, New Delhi, 2002; 2:275-295
4. Deng W, Yan Y, Zhuang P, Liu X, Tian K, Huang W, et al. Synthesis of nanocapsules blended polymeric hydrogel loaded with bupivacaine drug delivery system for local anesthetics and pain management. Drug Deliv. 2022; 29(1):399-412.
5. Chatur and Dhole Int. J. Pharm. Res. Allied Sci., 2022, 11(1): 99-107.
6. Das S, Subuddhi U. Controlled delivery of ibuprofen from poly (vinyl alcohol) − poly (ethylene glycol) interpenetrating polymeric network hydrogels. J Pharm Anal. 2019; 9(2):108-16.
7. Li J, Li X, Xie P, Liu P. Regulation of drug release performance using mixed doxorubicin-doxorubicin dimer nanoparticles as a pH-triggered drug self-delivery system. J Pharm Anal. 2022; 12(1):122-8.
8. Verma DD, Verma S, Blume G, Fahr A. Particle size of liposomes influences dermal delivery of substances into the skin. Int J Pharm. 2003; 258(1-2):141-51.
9. Peerzade MY, Memon S, Bhise K, Aamer AI. Development and validation of UV-Visible spectrophotometric method for estimation of ritonavir in bulk and formulation. Pharma Innovation J. 2019; 8:30-4.
10. Chaudhari SP, Bangar JV, Akuskar GK, Ratnaparkhi MP. Development and validation of UV spectrophotometric method for simultaneous estimation of rutin and quercetin in niosome formulation. Der Pharmacia Lettre. 2014;6(3):271-6.
11. ICH Harmonised Tripartite Guideline (1994) Text on Validation of Analytical Procedures. International Conference on Harmonization, Geneva, Switzerland, p. 1-5.
12. ICH Q1A (R2) (2003) Stability Testing of New Drug Substances and Products.
13. Konari SN, Jacob JT (2015) Application of Analytical Validated High-Performance Thin-Layer Chromatographic Technique for the Multicomponent Analysis of Cardiovascular Drug Combos in Pharmaceutical Dosage Form. J P C 28(5): 354-361.
14. ICH Q2 (R1) (2005) Validation of Analytical Procedures: Text and Methodology.