Program of Post-graduation in Pharmaceutical Sciences (FFEO/UFC), Federal University of Ceara, Ceara, Brazil.
Department of Pharmacy, Federal University of Ceara, Ceara, Brazil.
Curr Pharm Biotechnol. 2020;21(2):97-109. doi: 10.2174/1389201020666190621104624.
Venom-derived peptides display diverse biological and pharmacological activities, making them useful in drug discovery platforms and for a wide range of applications in medicine and pharmaceutical biotechnology. Due to their target specificities, venom peptides have the potential to be developed into biopharmaceuticals to treat various health conditions such as diabetes mellitus, hypertension, and chronic pain. Despite the high potential for drug development, several limitations preclude the direct use of peptides as therapeutics and hamper the process of converting venom peptides into pharmaceuticals. These limitations include, for instance, chemical instability, poor oral absorption, short halflife, and off-target cytotoxicity. One strategy to overcome these disadvantages relies on the formulation of bioactive peptides with nanocarriers. A range of biocompatible materials are now available that can serve as nanocarriers and can improve the bioavailability of therapeutic and venom-derived peptides for clinical and diagnostic application. Examples of isolated venom peptides and crude animal venoms that have been encapsulated and formulated with different types of nanomaterials with promising results are increasingly reported. Based on the current data, a wealth of information can be collected regarding the utilization of nanocarriers to encapsulate venom peptides and render them bioavailable for pharmaceutical use. Overall, nanomaterials arise as essential components in the preparation of biopharmaceuticals that are based on biological and pharmacological active venom-derived peptides.
毒液衍生肽具有多种生物和药理活性,使其成为药物发现平台的有用工具,并在医学和药物生物技术的广泛应用中具有潜力。由于其靶向特异性,毒液肽有可能被开发成生物制药,用于治疗各种健康状况,如糖尿病、高血压和慢性疼痛。尽管药物开发潜力巨大,但一些限制因素排除了肽直接作为治疗剂的使用,并阻碍了将毒液肽转化为药物的过程。这些限制包括例如化学不稳定性、口服吸收差、半衰期短和非靶向细胞毒性。一种克服这些缺点的策略是利用纳米载体来制备生物活性肽。现在有多种生物相容性材料可用作纳米载体,可以提高治疗性肽和毒液衍生肽的生物利用度,用于临床和诊断应用。越来越多的报道表明,已经用不同类型的纳米材料对分离的毒液肽和粗动物毒液进行了封装和配方,取得了有希望的结果。根据目前的数据,可以收集到大量关于利用纳米载体来封装毒液肽并使它们可用于药物用途的信息。总的来说,纳米材料是基于生物和药理活性毒液衍生肽的生物制药制备中的重要组成部分。