Abstract View

Author(s): Pankaj Kumar*1, Satyam Namdev2, Rimjhim Rajpoot3, Dr. Kuldeep Kumar Savita4

Email(s): 1pk419863@gmail.com

Address:

    Smt. Vidyawati college of pharmacy, Gora Machhiya , Jhansi, UP

Published In:   Volume - 4,      Issue - 9,     Year - 2025

DOI: https://doi.org/10.71431/IJRPAS.2025.4905  

 View HTML        View PDF

Please allow Pop-Up for this website to view PDF file.

ABSTRACT:
Psoriasis is a chronic autoimmune condition that results in the rapid growth of skin cells, causing red, scaly patches. Despite the availability of several treatments, including topical corticosteroids and biologics, managing psoriasis remains challenging due to side effects, non-compliance, and limited long-term efficacy. Dithranol, a widely used treatment for psoriasis, has proven effective due to its anti-inflammatory and antiproliferative properties. However, its clinical use is hindered by poor solubility, skin irritation, and staining of both the skin and clothing. This study aimed to develop a novel Dithranol-loaded ethosomal gel, which could enhance its solubility, stability, skin penetration, and therapeutic efficacy while minimizing irritation and side effects. Ethosomes are lipid-based nanocarriers made from phospholipids, cholesterol, and alcohol, which can improve the skin penetration of drugs and provide controlled, sustained release. Given these characteristics, ethosomes were chosen as the drug delivery system for this study to optimize the delivery of Dithranol and make it more effective for treating psoriasis. The study focused on developing a formulation that could not only improve drug absorption through the skin but also offer longer-lasting therapeutic effects. Compared to traditional Dithranol creams, the ethosomal gel showed superior therapeutic effects with fewer side effects, particularly skin irritation and burning sensations.

Cite this article:
Pankaj Kumar, Satyam Namdev, Rimjhim Rajpoot, Dr. Kuldeep Kumar Savita.Formulation and Evaluation of Dithranol Ethosomes for Psoriasis. IJRPAS. 2025; 4(9): 42-53.DOI: https://doi.org/https://doi.org/10.71431/IJRPAS.2025.4905


 

1.         Davidovici BB, Sattar N, Jörg PC, Puig L, Emery P, Barker JN, Van De Kerkhof P, Ståhle M, Nestle FO, Girolomoni G, Krueger JG. Psoriasis and systemic inflammatory diseases: potential mechanistic links between skin disease and co- morbid conditions. Journal of Investigative Dermatology. 2010 Jul 1;130(7):1785- 96.

2.   Vičić M, Kaštelan M, Brajac I, Sotošek V, Massari LP. Current concepts of psoriasis immunopathogenesis. International Journal of Molecular Sciences. 2021 Oct 26;22(21):11574.

3.         Kimball AB, Jacobson C, Weiss S, Vreeland MG, Wu Y. The psychosocial burden of psoriasis. American journal of clinical dermatology. 2005 Dec;6:383-92.

4.         Zhang Y, Dong S, Ma Y, Mou Y. Burden of psoriasis in young adults worldwide from the global burden of disease study 2019. Frontiers in Endocrinology. 2024 Feb 13;15:1308822.

5.         Gupta A, Bhalani S, Chopra A, Jabin F, Gaur A, Kukreja I, Roy A, Brooks L, Sulzicki M, Verma V, Pandey S. EPH142 Epidemiological Disease Burden and Cost of Illness of Psoriasis in the US. Value in Health. 2022 Jul 1;25(7):S460-1.

6.         Reynolds KA, Pithadia DJ, Lee EB, Clarey D, Liao W, Wu JJ. Generalized pustular psoriasis: a review of the pathophysiology, clinical manifestations, diagnosis, and treatment. Cutis. 2022 Aug 1;110(2 Suppl):19-25.

7.         Kammerau B, Zesch A, Schaefer H. Absolute concentrations of dithranol and triacetyl-dithranol in the skin layers after local treatment: in vivo investigations with four different types of pharmaceutical vehicles. Journal of Investigative Dermatology. 1975 Mar 1;64(3):145-9.

8.         Zhang H, Zhai Y, Wang J, Zhai G. New progress and prospects: The application of nanogel in drug delivery. Materials Science and Engineering: C. 2016 Mar 1;60:560-8.

9.         Murphy EA, Majeti BK, Mukthavaram R, Acevedo LM, Barnes LA, Cheresh DA. Targeted nanogels: a versatile platform for drug delivery to tumors. Molecular cancer therapeutics. 2011 Jun 1;10(6):972-82.

10.     Thabet Y, Elsabahy M, Eissa NG. Methods for preparation of niosomes: A focus on thin-film hydration method. Methods. 2022 Mar 1;199:9-15.

11.     Barupal AK, Gupta V, Ramteke S. Preparation and characterization of ethosomes for topical delivery of aceclofenac. Indian journal of pharmaceutical sciences. 2010 Sep;72(5):582.

12.     Jain A, Jain SK. In vitro release kinetics model fitting of liposomes: An insight. Chemistry and physics of lipids. 2016 Dec 1;201:28-40.

13.     Agarwal R, Katare OP, Vyas SP. Preparation and in vitro evaluation of liposomal/niosomal delivery systems for antipsoriatic drug dithranol. International journal of pharmaceutics. 2001 Oct 9;228(1-2):43-52.

14.     Fathalla D, Youssef EM, Soliman GM. Liposomal and ethosomal gels for the topical delivery of anthralin: preparation, comparative evaluation and clinical assessment in psoriatic patients. Pharmaceutics. 2020 May;12(5):446.

Related Images:



Recent Images



Neurological Complications among Pregnant and Post Partum Mothers in a Private Hospital, Yogyakarta, Indonesia
Review on Regulatory Affairs in Pharmaceutical Industry
Cucumber and Mint Soap: Preparation and Evaluation
Topical Delivery in Cosmetics: Enhancing Penetration and Bioavailability
Formulation and Evaluation of Polyherbal Soap
Gelatin: A Widely Used Pharmaceutical Excipient
Therapeutic insights into Saroglitazar: a dual PPAR- α/γ agonist targeting diabetic dyslipidaemia and NAFLD
A Comprehensive Review on Dyslipidemia and Obesity: Pathophysiology, Clinical Implications and Management Approaches
Antidiabetic Herbs and Polyherbal Antidiabetic Formulations –An Overview
Review on Clinical Research and Clinical Trials

Tags