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通过熔融沉积成型 3D 打印指导药物生产的制剂前研究。

Preformulation Studies to Guide the Production of Medicines by Fused Deposition Modeling 3D Printing.

机构信息

Laboratory of Food, Drug, and Cosmetics (LTMAC), School of Health Sciences, University of Brasilia, Brasília, DF, 70910-900, Brazil.

Faculty of Ceilândia, University of Brasília, Brasília, DF, 72220-900, Brazil.

出版信息

AAPS PharmSciTech. 2021 Nov 2;22(8):263. doi: 10.1208/s12249-021-02114-7.

Abstract

Fused deposition modeling (FDM) 3D printing has demonstrated high potential for the production of personalized medicines. However, the heating at high temperatures inherent to this process causes unknown risks to the drug product's stability. The present study aimed to assess the use of a tailored preformulation protocol involving physicochemical assessments, including the rheological profiles of the samples, to guide the development of medicines by FDM 3D printing. For this, polymers commonly used in FDM printing, i.e., high impact polystyrene (HIPS), polylactic acid (PLA), and polyvinyl alcohol (PVA), and their common plasticizers (mineral oil, triethyl citrate, and glycerol, respectively) were evaluated using the thermolabile model drug isoniazid (INH). Samples were analyzed by chemical and physical assays. The results showed that although the drug could produce polymorphs under thermal processing, the polymeric matrix can be a protective element, and no polymorphic transformation was observed. However, incompatibilities between materials might impact their chemical, thermal, and rheological performances. In fact, ternary mixtures of INH, PLA, and TEC showed a major alteration in their viscoelastic behavior besides the chemical changes. On the other hand, the use of plasticizers for HIPS and PVA exhibited positive consequences in drug solubility and rheologic behavior, probably improving sample printability. Thus, the optimization of the FDM 3D printing based on preformulation studies can assist the choice of compatible components and seek suitable processing conditions to obtain pharmaceutical products.

摘要

熔融沉积成型(FDM)3D 打印在个性化药物生产方面具有巨大潜力。然而,该工艺固有的高温加热会对药物产品的稳定性造成未知风险。本研究旨在评估使用定制的预配方方案,包括对样品进行物理化学评估,例如流变特性,以指导 FDM 3D 打印的药物开发。为此,评估了常用于 FDM 打印的聚合物,即高抗冲聚苯乙烯(HIPS)、聚乳酸(PLA)和聚乙烯醇(PVA),以及它们的常见增塑剂(矿物油、柠檬酸三乙酯和甘油),以热不稳定模型药物异烟肼(INH)为代表。通过化学和物理分析对样品进行了评估。结果表明,尽管药物在热加工过程中可能会产生多晶型物,但聚合物基质可以起到保护作用,未观察到多晶型物的转化。然而,材料之间的不相容性可能会影响它们的化学、热和流变性能。事实上,除了化学变化外,INH、PLA 和 TEC 的三元混合物的粘弹性行为也发生了重大变化。另一方面,HIPS 和 PVA 增塑剂的使用对药物溶解度和流变性能表现出积极影响,可能会提高样品的可打印性。因此,基于预配方研究的 FDM 3D 打印优化可以辅助选择兼容的成分并寻找合适的加工条件以获得药物产品。

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