{"title":"减少聚(D, l -乳酸-羟基乙酸)微球的残留溶剂水平:可扩展工业生产的路线图。","authors":"Somayeh Khanmohammadi, Samira Sadeghi, Samira Ansari, Milad Jafari-Nodoushan, Mahdieh Farhangi","doi":"10.1080/03639045.2025.2514214","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Poly (D, L-lactic-co-glycolic acid) (PLGA) microspheres have garnered significant attention as biocompatible and biodegradable carriers for sustained drug delivery. However, the production of PLGA microspheres typically involves organic solvents, such as ethyl acetate and benzyl alcohol. Residual solvents are undesirable given their potential toxicity and adverse effects on product stability. Effective solvent removal is critical for ensuring the safety and functionality of microspheres.</p><p><strong>Method: </strong>In this study, 12 formulations were designed by altering the conditions of solvent extraction, washing, and solvent evaporation steps to reduce residual solvents and determine critical parameters in process. Microspheres were evaluated based on residual solvent content, drug loading, size, morphology, moisture content, injectability, and release kinetics.</p><p><strong>Result: </strong>In five formulations (F06-F10), at least the residual amount of one organic solvent was significantly reduced. Prolonging the microspheres' residence time in ethanolic solution during the second extraction phase (F11) resulted in notable organic solvent reductions (ethyl acetate 93% and benzyl alcohol 60% compared to formulation F01). Further, these microparticles were spherical with a geometric diameter of 75.8 μm, a drug loading percentage of 33.7%, and a reasonable release profile, representing significant achievements.</p><p><strong>Conclusion: </strong>This study highlighted the importance of some modifications in preparing PLGA microspheres that have not been reported previously. These modifications greatly affected the residual solvent amount as well as other physicochemical properties of microspheres including size, morphology, and release profile. Overall, some practical methods could be used for feasible industrial production of PLGA microspheres.</p>","PeriodicalId":11263,"journal":{"name":"Drug Development and Industrial Pharmacy","volume":" ","pages":"1-10"},"PeriodicalIF":2.2000,"publicationDate":"2025-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Reducing residual solvent levels in poly (D, L-lactic-co-glycolic acid) microspheres: a roadmap for scalable industrial production.\",\"authors\":\"Somayeh Khanmohammadi, Samira Sadeghi, Samira Ansari, Milad Jafari-Nodoushan, Mahdieh Farhangi\",\"doi\":\"10.1080/03639045.2025.2514214\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>Poly (D, L-lactic-co-glycolic acid) (PLGA) microspheres have garnered significant attention as biocompatible and biodegradable carriers for sustained drug delivery. However, the production of PLGA microspheres typically involves organic solvents, such as ethyl acetate and benzyl alcohol. Residual solvents are undesirable given their potential toxicity and adverse effects on product stability. Effective solvent removal is critical for ensuring the safety and functionality of microspheres.</p><p><strong>Method: </strong>In this study, 12 formulations were designed by altering the conditions of solvent extraction, washing, and solvent evaporation steps to reduce residual solvents and determine critical parameters in process. Microspheres were evaluated based on residual solvent content, drug loading, size, morphology, moisture content, injectability, and release kinetics.</p><p><strong>Result: </strong>In five formulations (F06-F10), at least the residual amount of one organic solvent was significantly reduced. Prolonging the microspheres' residence time in ethanolic solution during the second extraction phase (F11) resulted in notable organic solvent reductions (ethyl acetate 93% and benzyl alcohol 60% compared to formulation F01). Further, these microparticles were spherical with a geometric diameter of 75.8 μm, a drug loading percentage of 33.7%, and a reasonable release profile, representing significant achievements.</p><p><strong>Conclusion: </strong>This study highlighted the importance of some modifications in preparing PLGA microspheres that have not been reported previously. These modifications greatly affected the residual solvent amount as well as other physicochemical properties of microspheres including size, morphology, and release profile. 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引用次数: 0
摘要
目的:聚(D, l -乳酸-羟基乙酸)(PLGA)微球作为一种生物相容性和可生物降解的持续给药载体已经引起了人们的广泛关注。然而,PLGA微球的生产通常涉及有机溶剂,如乙酸乙酯和苯甲醇。考虑到残留溶剂的潜在毒性和对产品稳定性的不利影响,它们是不可取的。有效的溶剂去除是确保微球安全性和功能性的关键。方法:通过改变溶剂萃取、洗涤、溶剂蒸发等步骤的条件,设计12个配方,减少溶剂残留量,确定工艺关键参数。微球的残留溶剂含量、载药量、大小、形态、水分含量、可注射性和释放动力学进行了评价。结果:5个剂型(F06 ~ F10)中至少有1种有机溶剂的残留量明显减少。在第二萃取阶段(F11),延长微球在乙醇溶液中的停留时间,与配方F01相比,有机溶剂减少显著(乙酸乙酯减少93%,苯甲醇减少60%)。这些微颗粒呈球形,几何直径为75.8 μm,载药率为33.7%,释放曲线合理,取得了显著的成果。结论:本研究强调了在制备PLGA微球过程中一些未被报道的修饰的重要性。这些修饰极大地影响了残留溶剂的量以及微球的其他物理化学性质,包括尺寸、形态和释放轮廓。总的来说,一些实用的方法可以用于可行的工业生产PLGA微球。
Reducing residual solvent levels in poly (D, L-lactic-co-glycolic acid) microspheres: a roadmap for scalable industrial production.
Objective: Poly (D, L-lactic-co-glycolic acid) (PLGA) microspheres have garnered significant attention as biocompatible and biodegradable carriers for sustained drug delivery. However, the production of PLGA microspheres typically involves organic solvents, such as ethyl acetate and benzyl alcohol. Residual solvents are undesirable given their potential toxicity and adverse effects on product stability. Effective solvent removal is critical for ensuring the safety and functionality of microspheres.
Method: In this study, 12 formulations were designed by altering the conditions of solvent extraction, washing, and solvent evaporation steps to reduce residual solvents and determine critical parameters in process. Microspheres were evaluated based on residual solvent content, drug loading, size, morphology, moisture content, injectability, and release kinetics.
Result: In five formulations (F06-F10), at least the residual amount of one organic solvent was significantly reduced. Prolonging the microspheres' residence time in ethanolic solution during the second extraction phase (F11) resulted in notable organic solvent reductions (ethyl acetate 93% and benzyl alcohol 60% compared to formulation F01). Further, these microparticles were spherical with a geometric diameter of 75.8 μm, a drug loading percentage of 33.7%, and a reasonable release profile, representing significant achievements.
Conclusion: This study highlighted the importance of some modifications in preparing PLGA microspheres that have not been reported previously. These modifications greatly affected the residual solvent amount as well as other physicochemical properties of microspheres including size, morphology, and release profile. Overall, some practical methods could be used for feasible industrial production of PLGA microspheres.
期刊介绍:
The aim of Drug Development and Industrial Pharmacy is to publish novel, original, peer-reviewed research manuscripts within relevant topics and research methods related to pharmaceutical research and development, and industrial pharmacy. Research papers must be hypothesis driven and emphasize innovative breakthrough topics in pharmaceutics and drug delivery. The journal will also consider timely critical review papers.