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异质成核对含有 Eudragit L10055 或 Acryl-EZE 的熔融挤出物中愈创甘油醚表面结晶的影响。

The influence of heterogeneous nucleation on the surface crystallization of guaifenesin from melt extrudates containing Eudragit L10055 or Acryl-EZE.

机构信息

PharmaForm, LLC, Austin, TX, United States.

出版信息

Eur J Pharm Biopharm. 2010 May;75(1):71-8. doi: 10.1016/j.ejpb.2009.12.001. Epub 2009 Dec 6.

Abstract

The objective of this study was to investigate the influence of talc and humidity conditions during storage on the crystal growth of guaifenesin on the surface of melt-extruded matrix tablets. Tablets consisted of the model drug guaifenesin in a matrix of either Acryl-EZE(R) or Eudragit(R) L10055 and either no talc, 25% or 50% talc. After processing, the hot-melt-extruded matrix tablets were supersaturated with amorphous guaifenesin, which resulted in the development of guaifenesin drug crystals on exposed surfaces of the tablet during storage (all tablets were stored at 24 degrees C). A previously developed, quantitative test was used to assay for surface guaifenesin. In tablets with a drug-to-polymer ratio of 19:81, talc-containing tablets exhibited an earlier onset of crystal growth (storage at 17% relative humidity). The presence of talc also increased the amount of surface crystallization and was independent of the talc concentration, since the talc levels used in this study exceeded the critical nucleant concentration. Additional non-melting components did not have an additive effect on surface crystal growth. High humidity during storage (78%) increased guaifenesin crystallization, but moisture uptake of tablets did not correlate with increased drug recrystallization. When storage at 17% relative humidity was interrupted for 3days by storage at 78% relative humidity before the tablets were returned to their previous low RH storage conditions, crystal growth quickly increased during the high RH interval and remained at an elevated level throughout the remaining storage period. A similar intermediate period of low, 17% relative humidity in tablets stored before and after that time at 78% RH did not affect surface crystallization levels. The effects of humidity and talc on the crystallization of guaifenesin from melt-extruded dosage forms supersaturated with amorphous drug were ascribed to heterogeneous nucleation.

摘要

本研究旨在探讨滑石粉的存在以及储存过程中的湿度条件对熔融挤出基质片中愈创甘油醚晶体生长的影响。研究采用模型药物愈创甘油醚,基质为 Acryl-EZE(R) 或 Eudragit(R) L10055,滑石粉的含量分别为 0、25%或 50%。熔融挤出后,基质片处于过饱和状态,其中无定形的愈创甘油醚会在储存过程中(所有片剂均在 24°C 下储存)在片剂暴露的表面上形成愈创甘油醚晶体。先前开发的定量检测方法用于检测表面愈创甘油醚的含量。在药物与聚合物的比例为 19:81 的片剂中,含有滑石粉的片剂晶体生长的起始时间更早(在相对湿度为 17%的条件下储存)。滑石粉的存在还增加了表面结晶的数量,且与滑石粉的浓度无关,因为本研究中使用的滑石粉水平超过了临界成核剂浓度。额外的非熔融成分对表面晶体生长没有附加影响。储存过程中的高湿度(78%)会增加愈创甘油醚的结晶,但片剂的水分吸收与药物的再结晶没有相关性。当片剂在 17%相对湿度下储存 3 天后切换到 78%相对湿度并在返回低 RH 储存条件之前,高 RH 间隔期间晶体生长迅速增加,并在整个剩余储存期内保持在较高水平。在此之前和之后在 78% RH 下储存一段时间,片剂处于相对湿度为 17%的中间低湿度期,但不会影响表面结晶水平。湿度和滑石粉对熔融挤出的超饱和无定形药物剂型中愈创甘油醚结晶的影响归因于异质成核。

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