Kusuma School of Biological Sciences, Indian Institute of Technology Delhi, New Delhi, 110016, India.
Genohelex Care Pvt. Ltd, ASPIRE BioNEST, University of Hyderabad, Hyderabad, Telangana, 500046, India.
Appl Microbiol Biotechnol. 2023 May;107(10):3153-3181. doi: 10.1007/s00253-023-12512-5. Epub 2023 Apr 13.
Effective delivery of drug molecules to the target site is a challenging task. In the last decade, several innovations in the drug delivery system (DDS) have tremendously improved the therapeutic efficacy of drug molecules. Among various DDS, cell-penetrating peptides (CPPs) based DDS have gathered notable attention owing to their safety, efficacy, selectivity, specificity, and ease of synthesis. CPPs are emerging as an efficient and effective pharmaceutical nanocarriers-based platforms for successful management of various important human health disorders. Failure of several current chemotherapeutic strategies is attributed to low solubility, reduced bioavailability, and off-target delivery of several anti-cancer drugs. Similarly, development of therapeutics for vision-threatening disorders is challenged by the anatomical as well as physiological complexity of the eye. Such therapeutic challenges in cancer and ocular disease management can be overcome by developing cell-penetrating peptide (CPP) based peptide drug conjugates (PDCs). CPPs can be used to deliver various types of cargo molecules including nucleic acids, small molecules, and peptides/proteinaceous agents. In this review, we have briefly introduced CPPs and the linker strategies employed for the development of PDCs. Furthermore, recent studies employing CPP-based PDCs for cancer and ocular disease management have been discussed in detail highlighting their significance over conventional DDS. Later sections of the review are focused on the current status of clinical trials and future implications of CPP-based PDCs in vaccine development. KEY POINTS: • Cell-penetrating peptides (CPPs) can deliver a variety of cargo macromolecules via covalent and non-covalent conjugation. • CPP-based peptide drug conjugates (PDCs) can overcome drawbacks of conventional drug delivery methods such as biocompatibility, solubility, stability, and specificity. • Various PDCs are in clinical trial phase for cancer and ocular therapeutics.
有效将药物分子递送到靶位是一项具有挑战性的任务。在过去的十年中,药物传递系统(DDS)的几项创新极大地提高了药物分子的治疗效果。在各种 DDS 中,基于细胞穿透肽(CPP)的 DDS 因其安全性、有效性、选择性、特异性和易于合成而引起了人们的极大关注。CPP 作为一种有效的药物纳米载体平台,正在成为成功管理各种重要人类健康疾病的平台。几种当前化疗策略的失败归因于几种抗癌药物的低溶解度、生物利用度降低和非靶向递送。同样,由于眼睛的解剖和生理复杂性,开发治疗视力威胁性疾病的疗法也具有挑战性。通过开发基于细胞穿透肽(CPP)的肽药物偶联物(PDC)可以克服癌症和眼部疾病管理中的这些治疗挑战。CPP 可用于递送各种类型的货物分子,包括核酸、小分子和肽/蛋白质药物。在本综述中,我们简要介绍了 CPP 及其用于开发 PDC 的连接子策略。此外,还详细讨论了最近使用 CPP 基 PDC 进行癌症和眼部疾病管理的研究,强调了它们相对于传统 DDS 的重要性。综述的后面部分侧重于 CPP 基 PDC 在疫苗开发中的当前临床试验状况和未来意义。
细胞穿透肽(CPP)可以通过共价和非共价缀合来递送各种货物大分子。
基于 CPP 的肽药物偶联物(PDC)可以克服传统药物递送方法的缺点,例如生物相容性、溶解度、稳定性和特异性。
各种 PDC 处于癌症和眼部治疗的临床试验阶段。