Design of Olanzapine/Lutrol Solid Dispersions of Improved Stability and Performances

Pharmaceutics

Cristina Cavallari¹  Adamo Fini¹ 

[1] Department FABIT, University of Bologna, Via San Donato 15, 40127 Bologna, Italy; E-Mail:

关键词: olanzapine;    solid dispersion;    Lutrol^® F68 and Lutrol^® F127;    Gelucire^® 44/14;    DSC;    HSM;    XRD;    stability;    accelerated release;   

DOI  :  10.3390/pharmaceutics5040570

来源: mdpi

【 摘 要 】

Eleven solid dispersions containing olanzapine, with carriers of different composition (Lutrol^® F68, Lutrol^® F127, Gelucire^® 44/14), were prepared and examined by thermal (differential scanning calorimetry (DSC); thermomicroscopy (HSM)) and X-ray diffraction (XRD) analysis, both as fresh or aged (one year) samples. Drug and carriers were preliminarily selected in order to avoid problems related to the aging of the formulation, according to the solubility parameters of carriers and drug. These parameters make it possible to predict the low solubility of olanzapine in the carriers (alone or in mixtures). Systems containing only Lutrol (also in the presence of Transcutol^®) contain the drug in the form of particles of reduced size and in a crystalline form. Gelucire^® 44/14 apparently increases the amount of olanzapine dissolved in the solid carrier, but this is presumed to be a metastable state, probably related to the heterogeneous nature of the carrier that delays crystallization of the drug. The high hydrophilicity of the carriers proves suitable to an accelerated and quick release of the drug regardless of aging. Differences in the release profiles between Lutrol- and Gelucire-containing systems were interpreted in terms of the formation of polymer micelles by the Lutrols when in aqueous solution.

【 授权许可】

CC BY   
© 2013 by the authors; licensee MDPI, Basel, Switzerland.