Exploration of Biogenic Nano-chemobiotics Fabricated by Silver Nanoparticle and Galactoxyloglucan with an Efficient Biodistribution in Solid Tumor Investigated by SERS Fingerprinting

被引:34
作者
Joseph, Manu M. [1 ,2 ]
Nair, Jyothi B. [1 ,4 ]
Adukkadan, Ramya N. [1 ,4 ]
Hari, Neethu [5 ]
Pillai, Raveendran K. [3 ]
Nair, Ananthakrishnan J. [5 ]
Maiti, Kaustabh Kumar [1 ,4 ]
Therakathinal, Sreelekha T. [2 ]
机构
[1] CSIR NIIST, Organ Chem Sect, CSTD, Thiruvananthapuram 695019, Kerala, India
[2] Lab Biopharmaceut & Nanomed, Div Canc Res, Thiruvananthapuram 695011, Kerala, India
[3] RCC, Clin Lab Serv, Thiruvananthapuram 695011, Kerala, India
[4] Acad Sci & Innovat Res AcSIR, New Delhi, India
[5] Univ Kerala, Dept Biotechnol, Thiruvananthapuram 695581, Kerala, India
关键词
cancer; galactoxyloglucan; surface-enhanced Raman scattering; nano-chemobiotics; antimicrobial; DRUG-DELIVERY; IMMUNOMODULATORY PROPERTIES; GOLD NANOPARTICLES; RAMAN-SPECTROSCOPY; MURINE ASCITES; CANCER-CELLS; IN-VITRO; SURFACE; DOXORUBICIN; TOXICITY;
D O I
10.1021/acsami.7b03191
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
An incredible exploration ensued of a dual modality nanocomposite wherein chemotherapy in fusion with antibacterial efficacy is obtained in a biogenic fabrication, which transformed as a novel nano-chemobiotics (NCB) prevailing fundamental molecular level investigation by surface-enhanced Raman scattering (SERS) platform. The nanocomposite is a facile, robust, and ecofriendly constitution between silver nanoparticles (SNPs) and a naturally occurring galactoxyloglucan (PST001) denoted as SNP@PST, which displayed biocompatibility with an upgraded selective cytotoxicity toward cancer cells. The relatively nontoxic nature of the SNP@PST on normal cells and red blood cells was further proved by detailed toxicological profiling on BALB/c mice. As a unique outcome, we observed excellent antibacterial activity, which is complementary to the greater cytotoxicity by the NCB. In diagnostic aspect, SNP@PST was revealed to be a superior SERS substrate with multiscale Raman signal enhancement contributed by homogeneous hot-spot distribution. Finally, the inherent SERS feature enabled us to investigate the biodistribution of the NCB in tumor-challenged mice using Raman fingerprinting and mapping analysis. Hence, the unrevealed SNP@PST orchestrated with the surfactant-free green method resembled a potential theransonstic NCB construct with synergistic anticancer and antibacterial potential in a single platform.
引用
收藏
页码:19578 / 19590
页数:13
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