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用于癌症细胞和组织生物成像的牛奶外泌体发光纳米系统

Milk Exosome-Glow Nanosystem for Cancer Cellular and Tissue Bioimaging.

作者信息

Cotto Nycol M, Chauhan Neeraj, Adriano Benilde, Chauhan Deepak S, Cabrera Marco, Chauhan Subhash C, Yallapu Murali M

机构信息

Division of Immunology and Microbiology, Medicine and Oncology Integrated Service Unit, School of Medicine, The University of Texas Rio Grande Valley, McAllen, Texas 78504, United States.

South Texas Center of Excellence in Cancer Research, School of Medicine, University of Texas Rio Grande Valley, McAllen, Texas 78504, United States.

出版信息

Chem Biomed Imaging. 2024 Aug 7;2(10):711-720. doi: 10.1021/cbmi.4c00040. eCollection 2024 Oct 28.

DOI:10.1021/cbmi.4c00040
PMID:39483633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11522989/
Abstract

Milk-derived exosomes are widely used for diagnosis, delivery, imaging, and theranostic applications. Near-Infrared (NIR) based fluorescence bioimaging is an attractive and safer technique that is used for clinical applications. However, almost all NIR imaging agents tend to have poor photostability, short half-life, nonspecific protein binding, and concentration-dependent aggregation(s). Therefore, there is an unmet clinical need to develop newer and safer modalities to package and deliver NIR imaging agents. Bovine milk exosomes are natural, biocompatible, safe, and efficient nanocarriers that facilitate the delivery of micro- and macromolecules. Herein, we developed an exosome-based NIR dye loaded nanoimaging formulation that offers improved solubility and photostability of NIR dye. Following the acetic acid based extracellular vesicle (EV) treatment method, we extracted the bovine milk exosomes from a variety of pasteurized grade milk. The EVs were screened for their physicochemical properties such as particle size and concentration and zeta potential. The stability of these exosomes was also determined under different conditions, including storage temperatures, pH, and salt concentrations. Next, indocyanine green, a model NIR dye was loaded into these exosomes (Exo-Glow) via a sonication method and further assessed for their improved fluorescence intensity and photostability using an IVIS imaging system. Initial screening suggested that size of the selected bovine milk exosomes was ∼100-135 nm with an average particle concentration of 5.8 × 10 particles/mL. Exo-Glow further demonstrated higher fluorescence intensity in cancer cells and tissues when compared to free dye. These results showed that Exo-Glow has the potential to serve as a safer NIR imaging tool for cancer cells/tissues.

摘要

源自牛奶的外泌体广泛应用于诊断、递送、成像及诊疗应用。基于近红外(NIR)的荧光生物成像技术是一种用于临床应用的、具有吸引力且更安全的技术。然而,几乎所有的近红外成像剂往往都具有光稳定性差、半衰期短、非特异性蛋白质结合以及浓度依赖性聚集等问题。因此,开发更新颖、更安全的方式来包装和递送近红外成像剂存在尚未满足的临床需求。牛乳外泌体是天然、生物相容性好、安全且高效的纳米载体,有助于小分子和大分子的递送。在此,我们开发了一种基于外泌体的负载近红外染料的纳米成像制剂,该制剂提高了近红外染料的溶解度和光稳定性。采用基于乙酸的细胞外囊泡(EV)处理方法,我们从多种巴氏杀菌级牛奶中提取了牛乳外泌体。对这些细胞外囊泡的物理化学性质进行了筛选,如粒径、浓度和zeta电位。还在不同条件下测定了这些外泌体的稳定性,包括储存温度、pH值和盐浓度。接下来,通过超声处理方法将一种典型的近红外染料吲哚菁绿负载到这些外泌体中(Exo-Glow),并使用IVIS成像系统进一步评估其增强的荧光强度和光稳定性。初步筛选表明,所选牛乳外泌体的大小约为100 - 135 nm,平均颗粒浓度为5.8×10个颗粒/mL。与游离染料相比,Exo-Glow在癌细胞和组织中进一步表现出更高的荧光强度。这些结果表明,Exo-Glow有潜力作为一种更安全的用于癌细胞/组织的近红外成像工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e2e/11522989/5fc09bdd9248/im4c00040_0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e2e/11522989/43cea8080505/im4c00040_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e2e/11522989/89265444a2e1/im4c00040_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e2e/11522989/8f7b4eda202e/im4c00040_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e2e/11522989/7c043723de14/im4c00040_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e2e/11522989/ac36760983f4/im4c00040_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e2e/11522989/95a8eb432eef/im4c00040_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e2e/11522989/c58f1989488d/im4c00040_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e2e/11522989/21d90dae005d/im4c00040_0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e2e/11522989/5fc09bdd9248/im4c00040_0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e2e/11522989/43cea8080505/im4c00040_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e2e/11522989/89265444a2e1/im4c00040_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e2e/11522989/8f7b4eda202e/im4c00040_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e2e/11522989/7c043723de14/im4c00040_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e2e/11522989/ac36760983f4/im4c00040_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e2e/11522989/95a8eb432eef/im4c00040_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e2e/11522989/c58f1989488d/im4c00040_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e2e/11522989/21d90dae005d/im4c00040_0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e2e/11522989/5fc09bdd9248/im4c00040_0009.jpg

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本文引用的文献

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