Synthesis and Evaluation of Polyethylene Glycol-4000-Co-Poly (AMPS) Based Hydrogel Membranes for Controlled Release of Mupirocin for Efficient Wound Healing

Author:

Minhas Muhammad Usman1ORCID,Ahmad Sarfaraz2,Khan Kifayat Ullah2,Sohail Muhammad3,Abdullah Orva4,Khalid Ikrima5,Malik Nadia Shamshad6

Affiliation:

1. College of Pharmacy, University of Sargodha, University Road Sargodha City, Punjab, Pakistan

2. Department of Pharmaceutics, Faculty of Pharmacy, The Islamia University of Bahawalpur, Punjab, Pakistan

3. Department of Pharmacy, COMSATS Institute of Information Technology, Abbottabad 22060, KPK, Pakistan

4. Hamdard Institute of Pharmaceutical Science, Hamdard University Islamabad, Pakistan

5. Faculty of Pharmaceutical Sciences, GC University Faisalabad, Punjab, Pakistan

6. Department of Pharmacy, Capital University of Science and Technology, Islamabad Pakistan

Abstract

Background: Chronic wound healing is a major challenge for the health care system around the globe. The current study was conducted to develop and characterize chemically cross-linked polyethylene glycol-co-poly (AMPS) hydrogel membranes to enhance the wound healing efficiency of antibiotic mupirocin (MP). Methods: Free radical polymerization technique was used to develop hydrogel membranes. In an aqueous medium, polymer PEG-4000 was cross-linked with the monomer 2-acrylamido-2-methylpropane sulfonic acid (AMPS) in the presence of initiators ammonium peroxide sulfate (APS) and sodium hydrogen sulfite (SHS). N, N-Methylene-bis-acrylamide (MBA) was used as a cross-linker in preparing hydrogel membranes. Developed membranes were spherical, transparent, and had elasticity. FTIR, TGA/DSC, and SEM were used to characterize the polymeric system. Swelling behavior, drug loading, and release pattern at pH of 5.5 and 7.4, irritation study, ex vivo drug permeation, and deposition study were also evaluated. Results: Formed membranes were spherical, transparent, and had elasticity. The formation of a stable polymeric network was confirmed by structural and thermal analysis. Evaluation of the drug permeability in the skin showed good permeation and retention capabilities. No irritancy to the skin was observed. Conclusion: Based on the results obtained, the present study concluded that the formulated stable network might be an ideal network for the delivery of mupirocin in skin infections.

Publisher

Bentham Science Publishers Ltd.

Subject

Pharmaceutical Science

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