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甲磺酸奥扎格雷酯的奇特案例:一种具有不同溶液和固体结构的两亲性抗疟药物。

The Curious Case of the OZ439 Mesylate Salt: An Amphiphilic Antimalarial Drug with Diverse Solution and Solid State Structures.

机构信息

Drug Delivery, Disposition and Dynamics , Monash Institute of Pharmaceutical Sciences , 381 Royal Parade , Parkville , Victoria 3052 , Australia.

Australian Synchrotron, ANSTO , 800 Blackburn Road , Clayton , Victoria 3168 , Australia.

出版信息

Mol Pharm. 2018 May 7;15(5):2027-2035. doi: 10.1021/acs.molpharmaceut.8b00173. Epub 2018 Mar 30.

Abstract

Efforts to develop orally administered drugs tend to place an exceptional focus on aqueous solubility as this is an essential criterion for their absorption in the gastrointestinal tract. In this work we examine the solid state behavior and solubility of OZ439, a promising single-dose cure for malaria being developed as the highly water-soluble mesylate salt. The aqueous phase behavior of the OZ439 mesylate salt was determined using a combination of small angle neutron and X-ray scattering (SANS and SAXS, respectively). It was found that this salt has low solubility at low concentrations with the drug largely precipitated in free base aggregates. However, with increasing concentration these crystalline aggregates were observed to dissociate into cationic micelles and lamellar phases, effectively increasing the dissolved drug concentration. It was also found that the dissolved OZ439 spontaneously precipitated in the presence of biologically relevant anions, which we attribute to the high lattice energies of most of the salt forms of the drug. These findings show that aqueous solubility is not always what it seems in the context of amphiphilic drug molecules and highlights that its use as the principal metric in selecting drug candidates for development can be perilous.

摘要

开发口服药物的努力往往特别关注水溶解度,因为这是其在胃肠道中吸收的基本标准。在这项工作中,我们研究了 OZ439 的固态行为和溶解度,OZ439 是一种有前途的单剂量疟疾治疗药物,正在作为高度水溶性的甲磺酸盐开发。使用小角中子和 X 射线散射(分别为 SANS 和 SAXS)的组合确定了 OZ439 甲磺酸盐的水相行为。结果发现,该盐在低浓度下溶解度低,药物主要以游离碱聚集体沉淀。然而,随着浓度的增加,这些晶状聚集体被观察到解离成阳离子胶束和层状相,从而有效地增加了溶解药物的浓度。还发现,在存在生物相关阴离子的情况下,溶解的 OZ439 会自发沉淀,我们将其归因于该药物的大多数盐形式的晶格能很高。这些发现表明,在两亲性药物分子的情况下,水溶解度并不总是表面上的那样,并且强调了将其用作选择候选药物进行开发的主要指标可能是危险的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8536/5941250/a3797f511f9c/mp-2018-00173w_0001.jpg

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