Evidence map›Paper›PMID 42371380›Full record

ArticleInflammopharmacology2026

Preclinical investigation of hydroxychloroquine loaded ethosomal gel for topical treatment of rheumatoid arthritis.

Pradip Nirbhavane, Deepak Mourya, Ankit Raj, Shivam K Chaudhari, Kalpesh R Patil, Shailesh Chalikwar, Kailas K Moravkar

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Article in Inflammopharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Pradip Nirbhavane *Amity Institute of Pharmacy, Amity University Haryana, Gurugram, 122413, India.
Deepak Mourya *Department of Industrial Pharmacy and Quality Assurance, R.C. Patel Institute of Pharmaceutical Education and Research, Shirpur, 425405, India.
Ankit RajOniosome Healthcare Pvt Ltd, SAS Nagar, Punjab, 160055, India.
Shivam K ChaudhariDepartment of Pharmacology, R.C. Patel Institute of Pharmaceutical Education and Research, Shirpur, 425405, India.
Kalpesh R PatilDepartment of Pharmacology, R.C. Patel Institute of Pharmaceutical Education and Research, Shirpur, 425405, India.
Shailesh Chalikwar *Department of Industrial Pharmacy and Quality Assurance, R.C. Patel Institute of Pharmaceutical Education and Research, Shirpur, 425405, India.
Kailas K Moravkar *Department of Industrial Pharmacy and Quality Assurance, R.C. Patel Institute of Pharmaceutical Education and Research, Shirpur, 425405, India. moravkarkailas1985@gmail.com.ORCID https://orcid.org/0000-0002-0269-1576

Funding

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6 · The paper itself

Abstract

purposeHydroxychloroquine (HCQ) has been used conventionally for the management of RA. However, due to its high dose and adverse effects associated with the long-term use, its therapeutic utility is often limited. This research was undertaken to develop an ethosomes based topical dosage form of HCQ, to improve the transdermal delivery of HCQ in patients with RA.

methodsEthosomes were developed by varying the concentration of ethanol, phospholipids and surfactants in the formulations. The developed ethosomal formulation was characterized for particle size, zeta potential, PDI, % entrapment efficiency, etc. Ethosomes were then incorporated into Carbopol gel and evaluated for in vitro drug release, ex vivo skin permeation and in vivo anti-inflammatory/anti-arthritic activity.

resultsThe ethosomes were nanometric in size (~ 210 nm), with a narrow particle size distribution (PDI =  ~ 0.25), zeta potential of around -30 mV, and high entrapment efficiency (~ 80%). The formulation exhibited controlled release of HCQ over time (~ 77% in 24 h) and improved permeation through the skin (~ 70% in 24 h) compared to conventional gel formulation. The in vivo studies demonstrated a significant decrease in the inflammatory symptoms of RA (~ 19% paw swelling inhibition compared to 22% for marketed gel) and the HCQ-loaded ethosomal gel was well tolerated by the skin with no signs of irritation. The stability studies indicated very slight drug loss (< 2%) at the end of 3 months, demonstration excellent stability of the formulation).

conclusionThe ethosomes based gel formulation of HCQ has a potential to serve as an alternative to the conventional oral dosage form of the drug for the better management of RA.

Indexed as

Antirheumatic AgentsArthritis, RheumatoidHydroxychloroquineAdministration, CutaneousAdministration, TopicalAnimalsDrug LiberationGelsHumansLiposomesMaleParticle SizeRatsSkinSkin AbsorptionAntirheumatic AgentsGelsHydroxychloroquineLiposomesEthosomesHydroxychloroquineRheumatoid arthritisTransdermal application

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.