pH-sensitive pHLIP® coated niosomes.

Q3 Biochemistry, Genetics and Molecular Biology
Molecular Membrane Biology Pub Date : 2016-05-01 Epub Date: 2017-08-09 DOI:10.1080/09687688.2017.1342969
Mohan C Pereira, Monica Pianella, Da Wei, Anna Moshnikova, Carlotta Marianecci, Maria Carafa, Oleg A Andreev, Yana K Reshetnyak
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引用次数: 12

Abstract

Nanomedicine is becoming very popular over conventional methods due to the ability to tune physico-chemical properties of nano vectors, which are used for encapsulation of therapeutic and diagnostic agents. However, the success of nanomedicine primarily relies on how specifically and efficiently nanocarriers can target pathological sites to minimize undesirable side effects and enhance therapeutic efficacy. Here, we introduce a novel class of targeted nano drug delivery system, which can be used as an effective nano-theranostic for cancer. We formulated pH-sensitive niosomes (80-90 nm in diameter) using nonionic surfactants Span20 (43-45 mol%), cholesterol (50 mol%) and 5 mol% of pH (Low) insertion peptide (pHLIP) conjugated with DSPE lipids (DSPE-pHLIP) or hydrophobic fluorescent dye, pyrene, (Pyr-pHLIP). In coating of niosomes, pHLIP was used as an acidity sensitive targeting moiety. We have demonstrated that pHLIP coated niosomes sense the extracellular acidity of cancerous cells. Intravenous injection of fluorescently labeled (R18) pHLIP-coated niosomes into mice bearing tumors showed significant accumulation in tumors with minimal targeting of kidney, liver and muscles. Tumor-targeting niosomes coated with pHLIP exhibited 2-3 times higher tumor uptake compared to the non-targeted niosomes coated with PEG polymer. Long circulation time and uniform bio-distribution throughout the entire tumor make pHLIP-coated niosomes to be an attractive novel delivery system.

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ph敏感的pHLIP®包被乳质体。
纳米医学正变得比传统方法更受欢迎,因为它能够调整纳米载体的物理化学性质,纳米载体用于治疗和诊断药物的包封。然而,纳米医学的成功主要取决于纳米载体如何特异性和高效地靶向病理部位,以最大限度地减少不良副作用并提高治疗效果。在此,我们介绍了一种新型的靶向纳米给药系统,它可以作为一种有效的纳米治疗癌症的药物。我们使用非离子表面活性剂Span20 (43-45 mol%)、胆固醇(50 mol%)和5mol % pH (Low)插入肽(pHLIP)与DSPE脂质(DSPE-pHLIP)或疏水荧光染料芘(Pyr-pHLIP)偶联,配制了pH敏感的niosomes(直径80-90 nm)。在膜质体的包被中,pHLIP被用作酸敏感的靶向片段。我们已经证明,phillip包被的粒体感知癌细胞的细胞外酸度。将荧光标记(R18) phillip包被的niosomes静脉注射到荷瘤小鼠体内,在肿瘤中有明显的积累,而对肾脏、肝脏和肌肉的靶向作用很小。与非靶向膜质体相比,涂有聚乙二醇聚合物的膜质体的肿瘤吸收率高2-3倍。长循环时间和均匀的生物分布在整个肿瘤使phillip包被乳质体成为一种有吸引力的新型给药系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Membrane Biology
Molecular Membrane Biology 生物-生化与分子生物学
CiteScore
4.80
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Cessation. Molecular Membrane Biology provides a forum for high quality research that serves to advance knowledge in molecular aspects of biological membrane structure and function. The journal welcomes submissions of original research papers and reviews in the following areas: • Membrane receptors and signalling • Membrane transporters, pores and channels • Synthesis and structure of membrane proteins • Membrane translocation and targeting • Lipid organisation and asymmetry • Model membranes • Membrane trafficking • Cytoskeletal and extracellular membrane interactions • Cell adhesion and intercellular interactions • Molecular dynamics and molecular modelling of membranes. • Antimicrobial peptides.
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