Investigation of the State of Hydration of a Non-Stoichiometric Hydrate in a Low Dose Formulation Using 19F Solid-State NMR

IF 3.7 3区 医学 Q2 CHEMISTRY, MEDICINAL
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引用次数: 0

Abstract

A variable or non-stoichiometric hydrate of GDC-4379 was developed into a formulated capsule with a 1% drug loading. The water content of this hydrate varied from 0-0.7 moles over the relative humidity (RH) range of 0-98% (25°C). Since a variable state of hydration coupled with rapid equilibration of lattice water with the environmental RH can lead to challenges in formulation development, an analytical method to directly and accurately determine the state of hydration of the active in such a low dose formulation was deemed necessary. Owing to its high selectivity and fast acquisition times, 19F solid-state NMR was effectively utilized to directly determine the lattice water content of the active in the formulated capsule. By correlating Δδ, the chemical shift difference between the isotropic peaks, with the relative humidity and ultimately the lattice water content, the state of hydration of GDC-4379 in the formulated capsule was experimentally determined as 0.63 moles of water/mole of anhydrate.
利用 19F 固态 NMR 研究低剂量制剂中的非均相水合物的水合状态。
GDC-4379 的可变水合物或非化学计量水合物被开发成药物含量为 1%的配方胶囊。在相对湿度(RH)为 0-98% (25°C) 的范围内,这种水合物的含水量在 0-0.7 摩尔之间变化。由于水合状态的变化以及晶格水与环境相对湿度的快速平衡会给制剂开发带来挑战,因此有必要采用一种分析方法来直接准确地测定这种低剂量制剂中活性物质的水合状态。19F 固态核磁共振具有高选择性和快速采集时间的特点,因此被有效地用于直接测定配制胶囊中活性物质的晶格水含量。通过将各向同性峰之间的化学位移差Δδ与相对湿度以及晶格水含量相关联,实验确定了配制胶囊中 GDC-4379 的水合状态为 0.63 摩尔水/摩尔无水物。
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来源期刊
CiteScore
7.30
自引率
13.20%
发文量
367
审稿时长
33 days
期刊介绍: The Journal of Pharmaceutical Sciences will publish original research papers, original research notes, invited topical reviews (including Minireviews), and editorial commentary and news. The area of focus shall be concepts in basic pharmaceutical science and such topics as chemical processing of pharmaceuticals, including crystallization, lyophilization, chemical stability of drugs, pharmacokinetics, biopharmaceutics, pharmacodynamics, pro-drug developments, metabolic disposition of bioactive agents, dosage form design, protein-peptide chemistry and biotechnology specifically as these relate to pharmaceutical technology, and targeted drug delivery.
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