DEVELOPMENT OF TERMINALIA CHEBULA LOADED ETHOSOMAL GEL FOR TRANSDERMAL DRUG DELIVERY

Authors

  • Fatima Grace X Department of Pharmaceutics, Faculty of Pharmacy, Sri Ramachandra Medical College and Research Institute, Porur, Chennai - 600 116, Tamil Nadu, India.
  • Suganya K Department of Pharmaceutics, Faculty of Pharmacy, Sri Ramachandra Medical College and Research Institute, Porur, Chennai - 600 116, Tamil Nadu, India.
  • Shanmuganathan S Department of Pharmaceutics, Faculty of Pharmacy, Sri Ramachandra Medical College and Research Institute, Porur, Chennai - 600 116, Tamil Nadu, India.

DOI:

https://doi.org/10.22159/ajpcr.2018.v11i12.20764

Keywords:

Ethosomal, Gel, Terminalia chebula, Ethanol, Transdermal delivery drug

Abstract

Objective: Oral route is the usual route of drug delivery which has many advantages such as easy delivery but has disadvantages such as poor bioavailability and tendency to produce rapid blood level spikes, such that there becomes a necessity for higher dose or recurrent dosing which becomes difficult for the patient and also high cost. Keeping all these drawbacks in concern, there arises a necessity for novel development of drug delivery with improved therapeutic efficacy and safety with targeted delivery such that size and number of doses could be reduced. This can be achieved by transdermal delivery which possesses several advantages such as avoids first-pass metabolism, eliminates gastrointestinal irritation reduces frequency of dosing, and rapid termination of drug action.

Methods: Dried fruits of Terminalia chebula were extracted and preliminary phytochemical evaluation was performed. Ethosome was prepared by cold method using soya lecithin. Ethosomal gel was prepared using carbopol as gelling agent and was evaluated.

Results and Discussion: The prepared gel was evaluated for its pharmaceutical properties and was found to be satisfactory. The in vitro drug diffusion of ethosomal gel showed better release compared with that of the gel with extract. In vitro anti-arthritic activity exhibited significant effect compared to that of the standard diclofenac.

Conclusion: Considering all the above-mentioned factors, the present study was aimed to develop a natural drug-loaded ethosomal gel for transdermal drug delivery, thereby permeation of drug can be enhanced compared with conventional dosage forms.

Downloads

Download data is not yet available.

Author Biographies

Fatima Grace X, Department of Pharmaceutics, Faculty of Pharmacy, Sri Ramachandra Medical College and Research Institute, Porur, Chennai - 600 116, Tamil Nadu, India.

Assistant Professor,Departmant of pharmaceutics

Suganya K, Department of Pharmaceutics, Faculty of Pharmacy, Sri Ramachandra Medical College and Research Institute, Porur, Chennai - 600 116, Tamil Nadu, India.

Student, Departmant of pharmaceutics

Shanmuganathan S, Department of Pharmaceutics, Faculty of Pharmacy, Sri Ramachandra Medical College and Research Institute, Porur, Chennai - 600 116, Tamil Nadu, India.

Professor,

Departmant of pharmaceutics

References

Dinesh D, Amit AR, Maria S, Awaroop RL, Mohd HG. Drug vehicle based approaches of penetration enhancement. Int J Pharm Pharm Sci 2009;1 Suppl 1:24-45.

Gangwar S, Singh S, Garg G. Ethosomes: A novel tool for drug delivery through the skin. J Pharm Res 2010;3 Suppl 4:688-91.

Rao Y, Zheng F, Zhang X, Gao J, Liang W. In vitro percutaneous permeation and skin accumulation of finasteride using vesicular ethosomal carriers. AAPS PharmSciTech 2008;9:860-5.

Verma DD, Fahr A. Synergistic penetration enhancement effect of ethanol and phospholipids on the topical delivery of cyclosporin A. J Control Release 2004;97:55-66.

Kumar KP, Radhika PR, Sivakumar T. Ethosomes-a priority in transdermal drug delivery. Int J Adv Pharm Sci 2010;1:111-21.

Touitou E, Dayan N, Levi-Schaffer F, Piliponsky A. A novel lipid vesicular system for enhanced delivery. J Lip Res 1998;8:113.

Nikalje AP, Tiwari S. Ethosomes: A novel tool for transdermal drug delivery. Int J Res Pharm Sci 2012;2 Suppl 1:1-20.

Anitha PS, Ramkanth K, Sankari UM, Alagusundaram K, Gnanapraksah P, Devaki DR, et al. Ethosomes-a noninvasive vesicular carrier for transdermal drug delivery. Int J Rev Life Sci 2011;1 Suppl 1:17-24.

World Health Organization. Traditional Medicine-Growing Needs and Potential. WHO Policy Perspectives on Medicine. No. 2. WHO/EBM/2002. Geneva: WHO; 2002.

CSIR. The wealth of India- A Dictionary of Indian Raw Materials and Industrial Products. Vol X. New Delhi: Publication and Information Directorate, CSIR; 2002. pp. 522-524.

Khandelwal KR. Practical Pharmacognosy Techniques and Experiments. 22 ed. Pune: Nirali Prakashan; 2012. p. 3.3-5.

Kokate CK, Purohit AP, Gokhale SB. Pharmacognosy. 48 ed. Pune: Nirali Prakashan; 2013. p. 7.4.

Patel S. Ethosomes: A promising tool for transdermal delivery of drug. Pharm Info Net 2007;5 Suppl 3:2007.

Sheer A, Chauhan M. Ethosomes as vesicular carrier for enhanced transdermal delivery of ketoconazole-formulation and evaluation. J Pharm Cosmetol 2011;1 Suppl 3:1-14.

Guy RH. Ethosomes and recent approach in transdermal drug delivery system. Int J Pharm 1985;6:112-6.

Panchagnula R, Pillai O, Nair VB, Ramarao P. Transdermal iontophoresis revisisted. Curr Opin Chem Bio 2000;4:468-73.

Mezei M, Gulasekharam V. Liposomes-a selective drug delivery system for the topical route of administration. Lotion dosage form. Life Sci 1980;26:1473-7.

Jain NK. Advances in Controlled and Novel Drug Delivery. 1st ed. New Delhi: CBS Publication; 2001. p. 428-51.

Touitou E. Composition of Applying Active Substance to or Through the Skin. US: Patent; 1998. p. 5540934.

Barry BW. Is transdermal drug delivery research still important today? Drug Discov Today 2001;6:967-71.

Biju SS, Sushama T, Mishra PR, Khar RK. Vesicular systems: An overview. Ind J Pharm Sci 2006;68:141-53.

Lopez-Pinto J.M, Gonzalez-Rodriguez M.L, Rabasco A.M. Effect of cholesterol and ethanol on dermal delivery from DPPC liposomes. Int J Pharm 2005;298:1-12.

Jain S, Tiwary AK, Sapra B, Jain NK. Formulation and evaluation of ethosomes for transdermal delivery of lamivudine. AAPS PharmSciTech 2007;8:E111.

Sheo DM, Sunil KP, Anish KG, Gyanendra KS, Ram CD. Formulation development and evaluation of ethosome of stavudine. Ind J Pharm Edu Res 2010;44 Suppl 1:102-8.

Bendas ER, Tadros MI. Enhanced transdermal delivery of salbutamol sulfate via ethosomes. AAPS PharmSciTech 2007;8:E107.

Jain S, Jain NK. Progress in Controlled and Novel Drug Delivery System. New Delhi: CBS Publishers and Distributors; 2004. p. 131-53.

Patel NA, Patel NJ, Patel RP. Formulation and evaluation of curcumin gel for topical application. Pharm Dev Technol 2009;14:80-9.

Garg A, Negi LM, Chauhan M. Gel containing ethosomal vesicles for transdermal delivery of aceclofenac. Int J Pharm Pharm Sci 2010;2 Suppl 2:102-8.

Brahmankar DM, Jaiswal SB. Biopharmaceutics and Pharmacokinetics a Treatise. 1st ed. New Delhi: Vallabh Prakashan; 2002. p. 337.

Chippada SC, Vangalapati M. Antioxidant, an anti-inflammatory and anti-arthritic activity of Centella asiatica extracts. J Chem Biol Phys Sci 2011;1 Suppl 2:260-9.

Pandey S. Various techniques for the evaluation of anti arthritic activity in animal models. J Adv Pharm Technol Res 2010;1:164-71.

Published

07-12-2018

How to Cite

Grace X, F., S. K, and S. S. “DEVELOPMENT OF TERMINALIA CHEBULA LOADED ETHOSOMAL GEL FOR TRANSDERMAL DRUG DELIVERY”. Asian Journal of Pharmaceutical and Clinical Research, vol. 11, no. 12, Dec. 2018, pp. 380-3, doi:10.22159/ajpcr.2018.v11i12.20764.

Issue

Section

Original Article(s)

Most read articles by the same author(s)