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结晶糖及其喷雾干燥形式的物理化学稳定性:对相对湿度的依赖性以及在粉末吸入器中的适用性。

Physicochemical stability of crystalline sugars and their spray-dried forms: dependence upon relative humidity and suitability for use in powder inhalers.

作者信息

Naini V, Byron P R, Phillips E M

机构信息

Barr Laboratories, Inc. Pomona, New York 10970, USA.

出版信息

Drug Dev Ind Pharm. 1998 Oct;24(10):895-909. doi: 10.3109/03639049809097269.

Abstract

Lactose, trehalose, sucrose, and mannitol were purchased in crystalline form and fractionated by sieving. Coarse (125-212 microns) and fine (44-74 microns) free-flowing fractions were selected as typical of drug carriers in dry-powder inhalers. In addition, one batch of each sugar was spray-dried to form a respirable powder (> 50% [w/w], < 5 microns). Both fractions and the spray-dried powders were characterized before and after storage for 30 days at < 23%, 23%, 52%, 75% and 93% relative humidity (RH) at 25 degrees C. Moisture uptake was determined by thermogravimetric analysis (TGA) validated by Karl Fischer titration. Sieve fractions (before storage at different RHs) and spray-dried materials (before and after storage) were further characterized by differential scanning calorimetry (DSC) and x-ray powder diffraction (XRPD). All crystalline sieve fractions (except sucrose at 93% RH) were stable at 25 degrees C and showed insignificant moisture uptake when exposed to each relative humidity for 30 days. Sucrose dissolved in sorbed moisture at 93% RH. Spray-dried lactose, sucrose, and trehalose, which were collected in the amorphous form, showed moisture uptake, without recrystallization, when held for 30 days at 23% RH. These sugars recrystallized as sintered masses and became undispersible at > or = 52% RH. Spray-dried mannitol was apparently 100% crystalline when collected directly from the spray-dryer; it did not show humidity-induced changes. The physicochemical behavior of each sugar form is discussed as it relates to the sugar's suitability as a powder-inhaler excipient, with both conventional and protein drugs.

摘要

乳糖、海藻糖、蔗糖和甘露醇均以结晶形式购得,并通过筛分进行分级。选择粗颗粒(125 - 212微米)和细颗粒(44 - 74微米)的自由流动级分作为干粉吸入器中典型的药物载体。此外,将每种糖的一批样品进行喷雾干燥以形成可吸入粉末(> 50% [w/w],< 5微米)。对这些级分和喷雾干燥粉末在25℃下相对湿度(RH)分别为< 23%、23%、52%、75%和93%的条件下储存30天前后进行了表征。通过经卡尔费休滴定法验证的热重分析(TGA)测定吸湿量。通过差示扫描量热法(DSC)和X射线粉末衍射(XRPD)对筛分级分(在不同RH下储存前)和喷雾干燥材料(储存前后)进行了进一步表征。所有结晶筛分级分(93% RH下的蔗糖除外)在25℃下均稳定,并且在暴露于每种相对湿度30天时吸湿量不显著。蔗糖在93% RH下溶解于吸附的水分中。以无定形形式收集的喷雾干燥乳糖、蔗糖和海藻糖在23% RH下保持30天时表现出吸湿现象,且无重结晶。这些糖重结晶为烧结块,在RH≥52%时变得不可分散。直接从喷雾干燥器收集的喷雾干燥甘露醇显然100%为结晶态;它未表现出湿度诱导的变化。讨论了每种糖形式的物理化学行为与该糖作为传统药物和蛋白质药物的干粉吸入剂辅料适用性之间的关系。

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