Cohen Jessica L, Almutairi Adah, Cohen Joel A, Bernstein Matt, Brody Steven L, Schuster Daniel P, Fréchet Jean M J
College of Chemistry, University of California, Berkeley, California 94720-1460, USA.
Bioconjug Chem. 2008 Apr;19(4):876-81. doi: 10.1021/bc700414j. Epub 2008 Mar 5.
Biopharmaceuticals, such as proteins and DNA, have demonstrated their potential to prevent and cure diseases. The success of such therapeutic agents hinges upon their ability to cross complex barriers in the body and reach their target intact. In order to reap the full benefits of these therapeutic agents, a delivery vehicle capable of delivering cargo to all cell types, both phagocytic and non-phagocytic, is needed. This article presents the synthesis and evaluation of a microparticle delivery vehicle capable of cell penetration and sub-cellular triggered release of an encapsulated payload. pH-sensitive polyacrylamide particles functionalized with a polyarginine cell-penetrating peptide (CPP) were synthesized. The incorporation of a CPP into the microparticles led to efficient uptake by non-phagocytic cells in culture. In addition, the CPP-modified particles showed no cytotoxic effects at concentrations used in this study. The results suggest that these particles may provide a vehicle for the successful delivery of therapeutic agents to various cell types.
生物制药,如蛋白质和DNA,已展现出预防和治疗疾病的潜力。这类治疗药物的成功取决于它们穿越体内复杂屏障并完整抵达靶点的能力。为了充分发挥这些治疗药物的益处,需要一种能够将药物输送到所有细胞类型(包括吞噬细胞和非吞噬细胞)的递送载体。本文介绍了一种能够穿透细胞并在细胞内触发释放封装 payload 的微粒递送载体的合成与评估。合成了用聚精氨酸细胞穿透肽(CPP)功能化的pH敏感聚丙烯酰胺颗粒。将CPP掺入微粒中导致培养中的非吞噬细胞有效摄取。此外,CPP修饰的颗粒在本研究使用的浓度下未显示出细胞毒性作用。结果表明,这些颗粒可能为将治疗药物成功递送至各种细胞类型提供一种载体。