Spencer R. Marsh, Claire E. Beard, Robert G. Gourdie
{"title":"Milk extracellular vesicles: A burgeoning new presence in nutraceuticals and drug delivery","authors":"Spencer R. Marsh, Claire E. Beard, Robert G. Gourdie","doi":"10.1002/btm2.10756","DOIUrl":null,"url":null,"abstract":"<p>Mammalian milk, a multifaceted developmental biofluid, has attracted new attention due to its diverse constituents and their implications for health and disease. Among these constituents, extracellular vesicles (EVs) have emerged as focal points of investigation. EVs, including exosomes and small EVs, have demonstrated biological activity in preclinical studies—including reports of enhancement of cognition and neural complexity, promotion of gastrointestinal development, barrier function and microbiome richness, the bolstering of immune response, and facilitation of musculoskeletal maturation in neonates. The richness of milk as a source of EVs is noteworthy, with hundreds of milliliters (at >10<sup>12</sup> EVs/mL) of nanovesicles extractable from a single liter of milk (>10<sup>14</sup> EVs/starting liter of milk). Techniques such as tangential flow filtration hold promise for scalable production, potentially extending to thousands of liters. Together with the scale and increasing sophistication of the dairy industry, the abundance of EVs in milk underscores their commercial potential in various nutraceutical applications. Beyond natural bioactivity, milk EVs (mEVs) present intriguing possibilities as orally deliverable, non-immunogenic pharmaceutical carriers, with burgeoning interest in their utilization for heart disease and cancer chemotherapy and as vectors for gene-editing modules such as CrispR. This review synthesizes current knowledge on mEV biogenesis, characterization, isolation methodologies, and cargo contents. Moreover, it delves into the therapeutic potential of mEVs, both as inherently bioactive nanovesicles and as versatile platforms for drug delivery. As efforts progress toward large-scale implementation, rigorous attention to safe, industrial-scale production and robust assay development will be pivotal in harnessing the translational promise of small EVs from milk.</p>","PeriodicalId":9263,"journal":{"name":"Bioengineering & Translational Medicine","volume":"10 3","pages":""},"PeriodicalIF":6.1000,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/btm2.10756","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioengineering & Translational Medicine","FirstCategoryId":"5","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/btm2.10756","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, BIOMEDICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Mammalian milk, a multifaceted developmental biofluid, has attracted new attention due to its diverse constituents and their implications for health and disease. Among these constituents, extracellular vesicles (EVs) have emerged as focal points of investigation. EVs, including exosomes and small EVs, have demonstrated biological activity in preclinical studies—including reports of enhancement of cognition and neural complexity, promotion of gastrointestinal development, barrier function and microbiome richness, the bolstering of immune response, and facilitation of musculoskeletal maturation in neonates. The richness of milk as a source of EVs is noteworthy, with hundreds of milliliters (at >1012 EVs/mL) of nanovesicles extractable from a single liter of milk (>1014 EVs/starting liter of milk). Techniques such as tangential flow filtration hold promise for scalable production, potentially extending to thousands of liters. Together with the scale and increasing sophistication of the dairy industry, the abundance of EVs in milk underscores their commercial potential in various nutraceutical applications. Beyond natural bioactivity, milk EVs (mEVs) present intriguing possibilities as orally deliverable, non-immunogenic pharmaceutical carriers, with burgeoning interest in their utilization for heart disease and cancer chemotherapy and as vectors for gene-editing modules such as CrispR. This review synthesizes current knowledge on mEV biogenesis, characterization, isolation methodologies, and cargo contents. Moreover, it delves into the therapeutic potential of mEVs, both as inherently bioactive nanovesicles and as versatile platforms for drug delivery. As efforts progress toward large-scale implementation, rigorous attention to safe, industrial-scale production and robust assay development will be pivotal in harnessing the translational promise of small EVs from milk.
哺乳动物乳汁是一种多方面的发育性生物液体,由于其成分的多样性及其对健康和疾病的影响而引起了新的关注。在这些成分中,细胞外囊泡(EVs)已成为研究的重点。EVs,包括外泌体和小EVs,已经在临床前研究中显示出生物活性,包括增强认知和神经复杂性,促进胃肠道发育,屏障功能和微生物组丰富度,增强免疫反应,促进新生儿肌肉骨骼成熟的报道。牛奶作为ev来源的丰富程度值得注意,从一升牛奶(每升牛奶1014 ev)中可提取数百毫升(1012 ev /mL)纳米囊泡。切向流过滤等技术有望实现大规模生产,可能会扩大到数千升。随着乳制品行业的规模和日益复杂,牛奶中丰富的电动汽车强调了它们在各种营养保健应用中的商业潜力。除了天然生物活性外,牛奶ev (mev)作为口服递送的非免疫原性药物载体呈现出有趣的可能性,人们对其在心脏病和癌症化疗中的应用以及作为基因编辑模块(如CrispR)的载体的兴趣日益浓厚。本文综述了目前关于mEV生物发生、表征、分离方法和货物内容的知识。此外,它还深入研究了mev的治疗潜力,既可以作为固有的生物活性纳米囊泡,也可以作为药物输送的多功能平台。随着大规模实施的努力取得进展,严格关注安全,工业规模生产和强大的检测开发对于利用牛奶中的小型电动汽车的转化前景至关重要。
期刊介绍:
Bioengineering & Translational Medicine, an official, peer-reviewed online open-access journal of the American Institute of Chemical Engineers (AIChE) and the Society for Biological Engineering (SBE), focuses on how chemical and biological engineering approaches drive innovative technologies and solutions that impact clinical practice and commercial healthcare products.