Overview of Antibody Drug Delivery

被引:110
作者
Awwad, Sahar [1 ,2 ,3 ]
Angkawinitwong, Ukrit [1 ]
机构
[1] UCL Sch Pharm, London WC1N 1AX, England
[2] Moorfields Eye Hosp NHS Fdn Trust, Biomed Res Ctr, NIHR, London EC1 V9EL, England
[3] UCL Inst Ophthalmol, London EC1 V9EL, England
基金
英国医学研究理事会;
关键词
antibodies; protein; pharmacokinetics; drug delivery; stability; ENDOTHELIAL GROWTH-FACTOR; NEONATAL FC-RECEPTOR; VEGF TRAP-EYE; MONOCLONAL-ANTIBODY; HALF-LIFE; THERAPEUTIC PROTEINS; INTRAOCULAR PHARMACOKINETICS; SUSTAINED-RELEASE; FUSION PROTEIN; POPULATION PHARMACOKINETICS;
D O I
10.3390/pharmaceutics10030083
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Monoclonal antibodies (mAbs) are one of the most important classes of therapeutic proteins, which are used to treat a wide number of diseases (e.g., oncology, inflammation and autoimmune diseases). Monoclonal antibody technologies are continuing to evolve to develop medicines with increasingly improved safety profiles, with the identification of new drug targets being one key barrier for new antibody development. There are many opportunities for developing antibody formulations for better patient compliance, cost savings and lifecycle management, e.g., subcutaneous formulations. However, mAb-based medicines also have limitations that impact their clinical use; the most prominent challenges are their short pharmacokinetic properties and stability issues during manufacturing, transport and storage that can lead to aggregation and protein denaturation. The development of long acting protein formulations must maintain protein stability and be able to deliver a large enough dose over a prolonged period. Many strategies are being pursued to improve the formulation and dosage forms of antibodies to improve efficacy and to increase the range of applications for the clinical use of mAbs.
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页数:24
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