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无针注射囊泡磷脂凝胶——克服半固体长效释放系统给药障碍的新方法。

Needle-Free Injection of Vesicular Phospholipid Gels-A Novel Approach to Overcome an Administration Hurdle for Semisolid Depot Systems.

作者信息

Breitsamer Michaela, Winter Gerhard

机构信息

Department of Pharmacy, Pharmaceutical Technology and Biopharmaceutics, Ludwig-Maximilians-University, Munich 81377, Germany.

Department of Pharmacy, Pharmaceutical Technology and Biopharmaceutics, Ludwig-Maximilians-University, Munich 81377, Germany.

出版信息

J Pharm Sci. 2017 Apr;106(4):968-972. doi: 10.1016/j.xphs.2016.12.020. Epub 2016 Dec 29.

Abstract

Vesicular phospholipid gels (VPGs) are depot formulations for the sustained release of drugs which are characterized by a high amount of phospholipids in the formulation. They consist of physiological excipients only and therefore display high biocompatibility. Their manufacture is simple, cheap, solvent free, and ideal for the processing of proteins and peptides because of the low stress on the molecule, for example, by elevated temperatures. One major hurdle of VPGs is their high viscosity which makes them hard to almost impossible to inject with conventional, thin needles used for subcutaneous administration. However, so far no data are published to overcome this administration challenge. In the present study, needle-free injection was investigated and successfully applied as a technology for the easy and elegant administration of VPGs. VPGs with different phospholipid content were injected with a Biojector 2000 into gelatin blocks and full thickness pig skin postmortem as in vitro models and the injection depth was determined after injection. The release behavior was tested after shearing the VPG with the device to evaluate the effect of shearing on the drug release from the formulation. No differences were observed when compared to an ejection with needle and syringe.

摘要

囊泡磷脂凝胶(VPGs)是用于药物缓释的长效制剂,其特点是制剂中含有大量磷脂。它们仅由生理辅料组成,因此具有高生物相容性。其制造简单、成本低、无溶剂,并且由于对分子的压力低,例如在高温下,非常适合蛋白质和肽的加工。VPGs的一个主要障碍是它们的高粘度,这使得几乎不可能用用于皮下给药的传统细针进行注射。然而,到目前为止,尚未发表克服这一给药挑战的数据。在本研究中,对无针注射进行了研究,并成功地将其作为一种便于且优雅地给药VPGs的技术应用。将不同磷脂含量的VPGs用Biojector 2000注射到明胶块和死后的猪全层皮肤中作为体外模型,并在注射后确定注射深度。在用该装置剪切VPG后测试其释放行为,以评估剪切对制剂中药物释放的影响。与用针头和注射器注射相比,未观察到差异。

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