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Co-amorphous system of Bifonazole for improved in-vitro permeation and antifungal activity
Bifonazole (BF), belonging to the newer class of antifungal drugs, is being widely explored for topical administration for fungal infections. It has proven to have better efficiency than other older drugs. However, it's low solubility poses a challenge in the formulation and, therefore, in the...
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Published in: | JCIS open (Amsterdam) 2024-07, Vol.14, p.100108, Article 100108 |
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creator | Shah, Devanshi S. Gurram, Sharda Gadlawar, Vitthal N. Jha, Durgesh K. Kamble, Siddhi P. Amin, Purnima D. |
description | Bifonazole (BF), belonging to the newer class of antifungal drugs, is being widely explored for topical administration for fungal infections. It has proven to have better efficiency than other older drugs. However, it's low solubility poses a challenge in the formulation and, therefore, in the drug product's efficacy. Intending to harness the benefits of the drug, the objective of the current study was to prepare a supersaturated system of the drug with a coformer. A co-amorphous system (CAS) of BF and citric acid (CA) was prepared using solvent evaporation to achieve better permeation and antimicrobial efficacy after topical application. The prepared system was evaluated for its solid-state properties by DSC, XRD, and FTIR. The theoretical values of the glass transition temperature, as calculated by the Gordon-Taylor equation, correlated well with the observations of the thermal analysis. The prepared system was dispersed in propylene glycol to perform in-vitro permeation studies wherein enhanced permeation properties were noted. The CAS showed better antifungal properties against A. niger owing to better release and solubility of the drug. Thus, It was concluded that a co-amorphous system of BF is a promising formulation strategy for topical drug delivery.
[Display omitted]
•Co-amorphous system of Bifonazole and citric acid were prepared.•Co-former concentration was optimized.•Strat-M® membrane was used for in-vitro permeation studies.•Formulations showed higher in-vitro permeation.•Antifungal efficacy of the developed formulations was higher. |
doi_str_mv | 10.1016/j.jciso.2024.100108 |
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[Display omitted]
•Co-amorphous system of Bifonazole and citric acid were prepared.•Co-former concentration was optimized.•Strat-M® membrane was used for in-vitro permeation studies.•Formulations showed higher in-vitro permeation.•Antifungal efficacy of the developed formulations was higher.</description><identifier>ISSN: 2666-934X</identifier><identifier>EISSN: 2666-934X</identifier><identifier>DOI: 10.1016/j.jciso.2024.100108</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Anti-fungal studies ; Bifonazole ; Co-amorphous system ; In-vitro permeation ; Strat-M ; Supersaturation</subject><ispartof>JCIS open (Amsterdam), 2024-07, Vol.14, p.100108, Article 100108</ispartof><rights>2024 The Authors</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2798-f8111ff16e5c5db1e1758df6165acc092c60833f4b72d72a5e0a384f183f74463</cites><orcidid>0000-0002-4366-4144</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S2666934X24000072$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3549,27924,27925,45780</link.rule.ids></links><search><creatorcontrib>Shah, Devanshi S.</creatorcontrib><creatorcontrib>Gurram, Sharda</creatorcontrib><creatorcontrib>Gadlawar, Vitthal N.</creatorcontrib><creatorcontrib>Jha, Durgesh K.</creatorcontrib><creatorcontrib>Kamble, Siddhi P.</creatorcontrib><creatorcontrib>Amin, Purnima D.</creatorcontrib><title>Co-amorphous system of Bifonazole for improved in-vitro permeation and antifungal activity</title><title>JCIS open (Amsterdam)</title><description>Bifonazole (BF), belonging to the newer class of antifungal drugs, is being widely explored for topical administration for fungal infections. It has proven to have better efficiency than other older drugs. However, it's low solubility poses a challenge in the formulation and, therefore, in the drug product's efficacy. Intending to harness the benefits of the drug, the objective of the current study was to prepare a supersaturated system of the drug with a coformer. A co-amorphous system (CAS) of BF and citric acid (CA) was prepared using solvent evaporation to achieve better permeation and antimicrobial efficacy after topical application. The prepared system was evaluated for its solid-state properties by DSC, XRD, and FTIR. The theoretical values of the glass transition temperature, as calculated by the Gordon-Taylor equation, correlated well with the observations of the thermal analysis. The prepared system was dispersed in propylene glycol to perform in-vitro permeation studies wherein enhanced permeation properties were noted. The CAS showed better antifungal properties against A. niger owing to better release and solubility of the drug. Thus, It was concluded that a co-amorphous system of BF is a promising formulation strategy for topical drug delivery.
[Display omitted]
•Co-amorphous system of Bifonazole and citric acid were prepared.•Co-former concentration was optimized.•Strat-M® membrane was used for in-vitro permeation studies.•Formulations showed higher in-vitro permeation.•Antifungal efficacy of the developed formulations was higher.</description><subject>Anti-fungal studies</subject><subject>Bifonazole</subject><subject>Co-amorphous system</subject><subject>In-vitro permeation</subject><subject>Strat-M</subject><subject>Supersaturation</subject><issn>2666-934X</issn><issn>2666-934X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9kE1LAzEQhoMoWGp_gZf8ga352M2mBw9a_CgUvCiIlzCbTWqW3U1JtoX66027Ip48DDMM8z688yJ0TcmcEipumnmjXfRzRlieNoQSeYYmTAiRLXj-fv5nvkSzGBtCCJOUMsEm6GPpM-h82H76XcTxEAfTYW_xvbO-hy_fGmx9wK7bBr83NXZ9tndD8HhrQmdgcL7H0NepBmd3_QZaDHpw6eZwhS4stNHMfvoUvT0-vC6fs_XL02p5t840Kxcys8kKtZYKU-iirqihZSFrK6goQGuyYFoQybnNq5LVJYPCEOAyt1RyW-a54FO0Grm1h0Ztg-sgHJQHp04LHzYKwuB0a5TQoEViQkUgt4WV0paipBUnJc8Jh8TiI0sHH2Mw9pdHiTqmrRp1Slsd01Zj2kl1O6pMenPvTFBRO9NrU7tg9JB8uH_13x7nidw</recordid><startdate>202407</startdate><enddate>202407</enddate><creator>Shah, Devanshi S.</creator><creator>Gurram, Sharda</creator><creator>Gadlawar, Vitthal N.</creator><creator>Jha, Durgesh K.</creator><creator>Kamble, Siddhi P.</creator><creator>Amin, Purnima D.</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-4366-4144</orcidid></search><sort><creationdate>202407</creationdate><title>Co-amorphous system of Bifonazole for improved in-vitro permeation and antifungal activity</title><author>Shah, Devanshi S. ; Gurram, Sharda ; Gadlawar, Vitthal N. ; Jha, Durgesh K. ; Kamble, Siddhi P. ; Amin, Purnima D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2798-f8111ff16e5c5db1e1758df6165acc092c60833f4b72d72a5e0a384f183f74463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Anti-fungal studies</topic><topic>Bifonazole</topic><topic>Co-amorphous system</topic><topic>In-vitro permeation</topic><topic>Strat-M</topic><topic>Supersaturation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shah, Devanshi S.</creatorcontrib><creatorcontrib>Gurram, Sharda</creatorcontrib><creatorcontrib>Gadlawar, Vitthal N.</creatorcontrib><creatorcontrib>Jha, Durgesh K.</creatorcontrib><creatorcontrib>Kamble, Siddhi P.</creatorcontrib><creatorcontrib>Amin, Purnima D.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>CrossRef</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>JCIS open (Amsterdam)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shah, Devanshi S.</au><au>Gurram, Sharda</au><au>Gadlawar, Vitthal N.</au><au>Jha, Durgesh K.</au><au>Kamble, Siddhi P.</au><au>Amin, Purnima D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Co-amorphous system of Bifonazole for improved in-vitro permeation and antifungal activity</atitle><jtitle>JCIS open (Amsterdam)</jtitle><date>2024-07</date><risdate>2024</risdate><volume>14</volume><spage>100108</spage><pages>100108-</pages><artnum>100108</artnum><issn>2666-934X</issn><eissn>2666-934X</eissn><abstract>Bifonazole (BF), belonging to the newer class of antifungal drugs, is being widely explored for topical administration for fungal infections. It has proven to have better efficiency than other older drugs. However, it's low solubility poses a challenge in the formulation and, therefore, in the drug product's efficacy. Intending to harness the benefits of the drug, the objective of the current study was to prepare a supersaturated system of the drug with a coformer. A co-amorphous system (CAS) of BF and citric acid (CA) was prepared using solvent evaporation to achieve better permeation and antimicrobial efficacy after topical application. The prepared system was evaluated for its solid-state properties by DSC, XRD, and FTIR. The theoretical values of the glass transition temperature, as calculated by the Gordon-Taylor equation, correlated well with the observations of the thermal analysis. The prepared system was dispersed in propylene glycol to perform in-vitro permeation studies wherein enhanced permeation properties were noted. The CAS showed better antifungal properties against A. niger owing to better release and solubility of the drug. Thus, It was concluded that a co-amorphous system of BF is a promising formulation strategy for topical drug delivery.
[Display omitted]
•Co-amorphous system of Bifonazole and citric acid were prepared.•Co-former concentration was optimized.•Strat-M® membrane was used for in-vitro permeation studies.•Formulations showed higher in-vitro permeation.•Antifungal efficacy of the developed formulations was higher.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.jciso.2024.100108</doi><orcidid>https://orcid.org/0000-0002-4366-4144</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Anti-fungal studies Bifonazole Co-amorphous system In-vitro permeation Strat-M Supersaturation |
title | Co-amorphous system of Bifonazole for improved in-vitro permeation and antifungal activity |
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