Kapila Laboratory, Orofacial Sciences Department, School of Dentistry, University of California, San Francisco (UCSF), San Francisco, CA, USA.
Nano-Cell Interaction Lab., Department of Tissue Biology and Biochemistry, Biology Institute, University of Campinas (UNICAMP), Campinas, SP, Brazil.
J Control Release. 2020 May 10;321:100-118. doi: 10.1016/j.jconrel.2020.02.001. Epub 2020 Feb 5.
Antimicrobial peptides (AMP) are molecules consisting of 12-100 amino acids synthesized by certain microbes and released extracellularly to inhibit the growth of other microbes. Among the AMP molecules, bacteriocins are produced by both gram-positive and gram-negative bacterial species and are used to kill or inhibit other prokaryotes in the environment. Due to their broad-spectrum antimicrobial activity, some bacteriocins have the potential of becoming the next generation of antibiotics for use in the crisis of multi antibiotic-resistant bacteria. Recently, bacteriocins have even been used to treat cancer. However, bacteriocins present a few drawbacks, such as sensitivity to proteases, immunogenicity issues, and the development of bacteriocin resistance by pathogenic bacteria. In this regard, nanoscale drug delivery systems (Nano-DDS) have led to the expectation that they will eventually improve the treatment of many diseases by addressing these limitations and improving bacteriocin pharmacokinetics and pharmacodynamics. Thus, combining bacteriocins with nano-DDS may be useful in overcoming these drawbacks and thereby reveal the full potential of bacteriocins. In this review article, we highlight the importance of tailoring nano-DDS to address bacteriocin limitations, the successes and failures of this technology thus far, the challenges that this technology still has to overcome before reaching the market, and future perspectives. Therefore, the purpose of this review is to highlight, categorize, compare and contrast the different nano-DDS described in the literature so far, and compare their effectiveness in order to improve the next generation of bacteriocin nano-sized drug delivery systems (Nano-DDS).
抗菌肽 (AMP) 是由某些微生物合成并释放到细胞外的分子,由 12-100 个氨基酸组成,用于抑制其他微生物的生长。在 AMP 分子中,细菌素由革兰氏阳性和革兰氏阴性细菌物种产生,用于杀死或抑制环境中的其他原核生物。由于其广谱抗菌活性,一些细菌素有可能成为下一代抗生素,用于应对多抗生素耐药菌的危机。最近,细菌素甚至被用于治疗癌症。然而,细菌素有一些缺点,如对蛋白酶的敏感性、免疫原性问题以及致病菌产生细菌素耐药性的问题。在这方面,纳米级药物递送系统 (Nano-DDS) 有望通过解决这些限制并改善细菌素的药代动力学和药效学,最终改善许多疾病的治疗效果。因此,将细菌素与纳米级药物递送系统结合使用可能有助于克服这些缺点,从而充分发挥细菌素的潜力。在这篇综述文章中,我们强调了定制纳米级药物递送系统以解决细菌素局限性的重要性,迄今为止该技术的成功和失败,该技术在进入市场之前仍需克服的挑战,以及未来的展望。因此,本综述的目的是突出、分类、比较和对比迄今为止文献中描述的不同纳米级药物递送系统,并比较它们的有效性,以改进下一代细菌素纳米级药物递送系统 (Nano-DDS)。