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Aljohani, M,MacFhionnghaile, P,McArdle, P,Erxleben, A
2019
April
International Journal Of Pharmaceutics
Investigation of the formation of drug-drug cocrystals and coamorphous systems of the antidiabetic drug gliclazide
Published
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Amorphous Antidiabetic Dissolution studies PHYSICAL STABILITY DISSOLUTION RATE MULTICOMPONENT CRYSTALS SOLID DISPERSIONS SOLUBILITY INDAPAMIDE ENHANCEMENT COFORMER
561
35
42
The antidiabetic drug gliclazide (GLZ) has a slow absorption rate and a low bioavailability due to its poor solubility. GLZ is often prescribed along with an antihypertensive, as many diabetic patients have coexistent hypertension. Cocrystallization and coamorphization are attractive strategies to enhance dissolution rates and to reduce the number of medications a patient has to take. In this work the formation of cocrystals and coamorphous systems of GLZ with various antihypertensive drugs was studied, namely chlorothiazide (CTZ), hydrochlorothiazide (HTZ), indapamide (IND), triamterene (TRI) and nifedipine (NIF) as well as benzamidine (BZA) as a model for the amidine pharmacophore. TRI, IND and HTZ were found to form coamorphous systems with GLZ that are stable for at least six months at 22 +/- 2 degrees C and 56% relative humidity. Coamorphous GLZ-TRI is also stable in dissolution medium. Coamorphization of GLZ-TRI with 15% sodium taurocholate gave a viable coamorphous formulation with an enhanced dissolution rate. Comilling of GLZ with BZA and cocrystallization from solution gave the amorphous and crystalline salt, respectively and the X-ray structure is reported. During attempts to obtain X-ray suitable cocrystals crystals of Na(+)GLZ(+) and IND 0.5H(2)O were obtained. Redetermination of the published structure of IND 0.5H(2)O revealed a unit cell with the length of the a axis doubled, a different space group and no disorder. Liquid-assisted grinding of a 1:1 mixture of GLZ and IND indicated the transformation of IND to a new solid-state form, while GLZ remained unaltered. Milling- and heating-induced solid-state transformations of IND are discussed.
10.1016/j.ijpharm.2019.02.024
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