Chitosan-based Mupirocin and Alkanna tinctoria extract nanoparticles for the management of burn wound: In vitro and in vivo characterization

Author:

Alam Shah Muhammad Khurshid1,Nawaz Asif1,Latif Muhammad Shahid1,Ullah Wasi1,Ullah Aziz2,Khan Azmat Ali3,Malik Abdul4,Kumarasamy Vinoth5,Subramaniyan Vetriselvan6,Azad Abul Kalam7

Affiliation:

1. Advance Drug Delivery Lab, Gomal Center of Pharmaceutical Sciences, Faculty of Pharmacy, Gomal University , Dera Ismail Khan , 29050, KP , Pakistan

2. Department of Chemical Engineering, Pukyong National University , Busan 48513 , Republic of Korea

3. Pharmaceutical Biotechnology Laboratory, Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University , Riyadh 11451 , Saudi Arabia

4. Department of Pharmaceutics, College of Pharmacy, King Saud University , Riyadh 11451 , Saudi Arabia

5. Department of Parasitology and Medical Entomology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Jalan Yaacob Latif , 56000 Cheras , Kuala Lumpur , Malaysia

6. Department of Medical Sciences, School of Medical and Life Sciences, Sunway University, 47500 Selangor Darul Ehsan , Malaysia

7. Faculty of Pharmacy, University College of MAIWP International, 68100 Batu Caves , Kuala Lumpur , Malaysia

Abstract

Abstract Serious consequences including septicemia and amputations can result from complex wounds, which is a serious healthcare concern. In addition, there are currently only a few choices for management, which justifies the search for novel, highly effective wound-healing medications. This research work was aimed at fabricating chitosan-based Alkanna tinctoria and Mupirocin nanoparticles by ionic gelation technique for burn wound management. Preliminary studies were conducted, and the prepared nanoparticles were characterized by various techniques that involve, high-performance liquid chromatography for the detection of components in A. tinctoria root extract, ATR-FTIR, particle size, zeta potential, percent drug content (DC%), percent entrapment efficiency (EE%), scanning electron microscopy, and transmission electron microscopy (TEM) for surface morphology. The optimized formulation CS-AT-MU-NPs3 shows a particle size of 340.8 ± 34.46 nm and positive zeta potential 27.3 ± 3.10 mV. In vitro drug release study was also performed, which demonstrated improved and controlled release of the drug from the nanoparticles. The CS-AT-MU-NPs3 exhibited a maximum release up to 92.61% (AT) and 88.35% (MU). Antibacterial and antifungal activities of the formulation were also accessed by utilizing the agar well diffusion technique. The combination of AT and MU in chitosan-based nanoparticles was significantly effective against bacterial and fungal strains like Staphylococcus aureus, Pseudomonas aeruginosa, and Candida albicans as compared to other formulations. The skin irritation study was also conducted, which shows that the prepared formulation did not cause any observable changes to the skin in terms of inflammation, erythema, edema, or any other symptoms associated with skin irritation. All the chitosan-based nanoparticles showed almost 75% reduction in wound contraction, while the optimized formulation CS-AT-MU-NPs3 showed complete wound healing on the 15th day. Based on the results, it can be assumed that chitosan-based nanoparticles containing A. tinctoria and Mupirocin demonstrated good wound healing and could be used to effectively manage burn wounds of any description.

Publisher

Walter de Gruyter GmbH

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