Development and Characterization of topical microemulsion as novel drug delivery system for Dapsone
DOI:
https://doi.org/10.37285/ijpsn.2022.15.1.8Abstract
Dapsone is a Biopharmaceutical Classification System class II drug with anti inflammatory, immunosuppressive, antibacterial, and antibiotic properties and is used as an antileprotic. The purpose of the present study was to investigate the potential of a microemulsion formulation for topical delivery of dapsone to enhance permeation and to avoid systemic side effects. When administered orally, dapsone undergoes hepatic metabolism. Its hepatic metabolite, dapsone hydroxylamine, shows systemic side effects such as hemolytic anaemia peripheral neuropathy, nausea, and headache. A novel drug delivery system in the form of a microemulsion was developed for dapsone. This is the first attempt that dapsone has been combined with chaulmoogra oil in a topical microemulsion. The primary drugs used for the treatment of leprosy are found in chaulmoogra seeds. Considering its good solubilizing capacity and its use in the treatment of leprosy, chaulmoogra oil was chosen as the oil phase. Based on emulsification ability, Cremophor RH40 and PEG 400 were selected as surfactant and co-surfactant, respectively. A pseudo-ternary phase diagram was constructed to identify the microemulsion region. Smix (Cremophor RH40: PEG-400 in the ratio of 1:2) was most effective in imparting stability to the formulation. The selected formulation exhibited appropriate diffusion behavior (in vitro). The developed dapsone containing microemulsion formulation exhibited the optimal homogeneity, clarity, pH, type of microemulsion, viscosity, percent drug content, and percent transmittance to qualify as a topical drug delivery system for local treatment of leprosy.
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Keywords:
Microemulsion, Dapsone, Anti mycobacterial activity, Topical drug delivery system, Chaulmoogra oil, HET-CAM testDownloads
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Butani D, Yewale C, and Misra A (2014). Amphotericin B topical microemulsion: Formulation, characterization and evaluation. Colloids Surf B Biointerfaces 116: 351-358
Chaves LL, Silveri A, Vieira ACC, Ferreira D, Cristiano MC, Paolino D, Marzio LD, Lima SC, Reis S, Sarmento B, and Celia C (2019). pH-responsive chitosan based hydrogels affect the release of dapsone: Design, set-up, and physicochemical characterization. Int. J. Biol. Macromol. 133: 1268–1279
Coneac G, Vlaia V, Olariu I, Muţ AM, Anghel D F, Ilie C, Popoiu C, Lupuleasa D, and Vlaia L (2015). Development and evaluation of new microemulsion-based hydrogel formulations for topical delivery of fluconazole. AAPS
PharmSciTech 16(4): 889-904.
Hashem FM, Shaker DS, Ghorab MK, Nasr M, Ismail A (2011). Formulation, characterization, and clinical evaluation of microemulsion containing Clotrimazole for topical delivery. AAPS PharmSciTech, 12(3): 879-86.
Kweon JH, Chi SC, and Park ES (2004) Transdermal Delivery of Diclofenac Using Microemulsions, Arch Pharm Res 27 (3): 351-356.
Melby MA, and Laura AV (2012). The use of the microplate alamar blue assay (MABA) to assess the susceptibility of Mycobacterium lepraemurium to anti-leprosy and other drugs. J Infect Chemother 18: 652–661.
MerajAnjum Md, Kanoujia J, Parashar P, Arya M, Yadav AK, and Saraf S (2016). A evaluation of a Polymer-Lipid Polymer system utilizing hybrid nanoparticles of dapsone as a novel antiacne agent. Curr. Drug ther. 11: 86-100.
Monteiro LM, Lione VF, Carmo FA, Amaral LH, Silva JH, Nasciutti LE (2012). Development and characterization of a new oral Dapsone nanoemulsion system: permeability and in silico bioavailability studies. Int. J. Nanomed. 7: 5175– 5182.
Nithya R, Jerold P, Siram K (2018). Cubosomes of dapsone enhanced permeation across the skin. J. Drug Deliv. Sci. Technol. 48: 75–81.
Norton SA (1994). Useful plants of dermatology Hydnocarpus and chaulmoogra. J Am Acad Dermatol 31(4): 683-686.
Pal D, Chandra P, Sachan N (2020).Sesame Seed in Controlling Human Health and Nutrition in: Preedy V. R. Watson R. R. (Eds.), Nuts and Seeds in Health and Disease Prevention (Second Edition) pp 183-210
Saonere JA (2011) Leprosy: An overview. J. Infect. Dis. Immun.; 3 (14): 233-2043.
Shah R, Magdum C, and Wadkar K (2009). Fluconazole topical microemulsion: preparation and evaluation. Research J. Pharm. and Tech. 2: 353-357.
Shamma RN, Ad-din IS, and Abdeltawabb N F (2019). Dapsone- gel as a novel platform for acne treatment: In vitro evaluation and In vivo performance and histopathological studies in acne infected mice. J. Drug Deliv. Sci. Technol.
:101238.
Shinde U, Pokharkar S, and Modani S (2012). Design and Evaluation of Microemulsion Gel System of Nadifloxacin. Indian J. Pharm. Sci. 74 (3): 237-246.
Shukla T, Upmanyua N, Agrawal M, Saraf Sh, Saraf S, and Alexander A (2018). Biomedical applications of microemulsion through dermal and transdermal route. Biomedicine and Pharmacotherapy108:1477-1494.
Velpandian T, Bankoti R, Humayun S, Ravi AK, Kumari SS, and Biswas NR, (2006). Comparative evaluation of possible ocular photochemical toxicity of fluoroquinolones meant for ocular use in experimental models. Ind. J. Exp. Biol. 5: 387.
Vu S, Lams A, and Blomkalns A (2019). Neutropenia, Hypoxia, and the complexities of emergency medicine: A case of Dapsone-Induced Methemoglobinemia. J.Emerg. Med. 56(4): e47-e49.