Meola Tahlia R, Paxton Kara, Joyce Paul, Schultz Hayley B, Prestidge Clive A
UniSA: Clinical and Health Sciences, University of South Australia, City West Campus, Adelaide, South Australia 5000, Australia.
ARC Centre of Excellence in Convergent Bio-Nano Science & Technology, University of South Australia, City West Campus, Adelaide, South Australia 5000, Australia.
ADMET DMPK. 2020 Jul 17;8(4):437-451. doi: 10.5599/admet.830. eCollection 2020.
Lipid-based formulations (LBFs) are well-known to improve the oral bioavailability of poorly water-soluble drugs (PWSDs) by presenting the drug to the gastrointestinal environment in a molecularly dispersed state, thus avoiding the rate-limiting dissolution step. Risperidone and lurasidone are antipsychotics drugs which experience erratic and variable absorption, leading to a low oral bioavailability. The aim of this research was to develop and investigate the performance of risperidone and lurasidone when formulated as an emulsion and silica-lipid hybrid (SLH). Lurasidone and risperidone were dissolved in Capmul® MCM at 100% and 80% their equilibrium solubility, respectively, prior to forming a sub-micron emulsion. SLH microparticles were fabricated by spray-drying a silica stabilised sub-micron emulsion to form a solid powder. The performances of the formulations were evaluated in simulated intestinal media under digesting conditions, where the emulsion and SLH provided a 17-fold and 23-fold increase in LUR solubilisation, respectively. However, the performance of RIS was reduced by 2.2-fold when encapsulated within SLH compared to pure drug. Owing to its pKa, RIS adsorbed to the silica and thus, dissolution was significantly hindered. The results reveal that LBFs may not overcome the challenges of all PWSDs and physiochemical properties must be carefully considered when predicting drug performance.
基于脂质的制剂(LBFs)通过将药物以分子分散状态呈现于胃肠道环境中,从而避免限速溶解步骤,进而提高难溶性药物(PWSDs)的口服生物利用度,这是众所周知的。利培酮和鲁拉西酮是抗精神病药物,其吸收不稳定且变化较大,导致口服生物利用度较低。本研究的目的是开发并研究利培酮和鲁拉西酮制成乳剂和硅脂杂化物(SLH)时的性能。在形成亚微米乳剂之前,将鲁拉西酮和利培酮分别以其平衡溶解度的100%和80%溶解于Capmul® MCM中。通过喷雾干燥二氧化硅稳定的亚微米乳剂以形成固体粉末来制备SLH微粒。在模拟肠道介质的消化条件下评估制剂的性能,其中乳剂和SLH分别使鲁拉西酮的增溶量提高了17倍和23倍。然而,与纯药物相比,当利培酮被包封在SLH中时,其性能降低了2.2倍。由于其pKa,利培酮吸附到二氧化硅上,因此溶解受到显著阻碍。结果表明,基于脂质的制剂可能无法克服所有难溶性药物的挑战,在预测药物性能时必须仔细考虑其理化性质。