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<xml><ArticleSet><Article><Journal><PublisherName>Radiance Research Academy</PublisherName><JournalTitle>International Journal of Current Research and Review</JournalTitle><PISSN>2231-2196</PISSN><EISSN>0975-5241</EISSN><Volume/><Issue/><IssueLanguage>English</IssueLanguage><SpecialIssue>N</SpecialIssue><PubDate><Year>2026</Year><Month>June</Month><Day>15</Day></PubDate></Journal><ArticleType>Healthcare</ArticleType><ArticleTitle>&#xD;
	Formulation, Optimization, and Evaluation of Liposomal Amphotericin B for Improved Antifungal Therapy&#xD;
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</ArticleTitle><ArticleLanguage>English</ArticleLanguage><FirstPage>01</FirstPage><LastPage>07</LastPage><AuthorList><Author>Priti Gupta</Author><AuthorLanguage>English</AuthorLanguage><Author> Manali Rai</Author><AuthorLanguage>English</AuthorLanguage><Author> Saket Singh Chandel</Author><AuthorLanguage>English</AuthorLanguage></AuthorList><DOI>https://doi.org/10.31782/IJCRR.2026.181101</DOI><Abstract>&#xD;
	Background: Amphotericin B (AmB) remains a first-line therapeutic agent due to its broad-spectrum fungicidal activity and low microbial resistance. However, conventional formulations are severely restricted by dose-limiting nephrotoxicity driven by drug self-aggregation. Nanotechnology-driven drug delivery systems, particularly liposomes (L), have been widely adopted to over come these biopharmaceutical constraints. Objectives: This research aimed to formulate and optimize L-AmB using the thin-film hydration method to enhance drug stabil ity and reduce systemic toxicity, achieving high entrapment efficiency and controlled release through precise lipid-to-drug ratio modulation. Methods: L-AmB was prepared using HSPC, DSPG, and cholesterol via thin-film hydration. Preformulation studies included organoleptic evaluation, solubility analysis, melting point determination, and drug-excipient compatibility via FT-IR and DSC. The optimized formulation was characterized through standard methods. Results: The optimized formulation (Batch F4) exhibited a mean particle size of 82.4 &#xB1; 2.1 nm with a PDI of 0.142 and zeta potential of -32.5 &#xB1; 1.2 mV, indicating excellent physical stability. Entrapment efficiency reached 94.2 &#xB1; 1.5% with 92.8% yield. In vitro release studies demonstrated a sustained profile following the Higuchi model, with only 22% drug released in the first 8 hours. Stability studies confirmed refrigeration (4&#xB0;C) as optimal for maintaining liposomal integrity. Conclusions: The optimized L-AmB formulation represents a safer alternative to conventional deoxycholate treatments. The sub-micron size ensures long-term stability and enhanced circulation via EPR effect. The sustained release profile minimizes the &#x201C;burst effect&#x201D; associated with nephrotoxicity. This study demonstrates that L-AmB offers a promising platform for improved clinical outcomes in systemic fungal infections.&#xD;
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</Abstract><AbstractLanguage>English</AbstractLanguage><Keywords>Liposomes, Amphotericin B, Invasive Fungal Infections, Drug Delivery Systems, Nephrotoxicity, Nanocarriers, Thin-Film &#xD;
Hydration.</Keywords><URLs><Abstract>http://ijcrr.com/abstract.php?article_id=4911</Abstract><Fulltext>http://ijcrr.com/article_html.php?did=4911</Fulltext></URLs><References>&#xD;
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