| dc.contributor.author | Joseph, M M | |
| dc.contributor.author | Nair, J B | |
| dc.contributor.author | Maiti, K K | |
| dc.contributor.author | Sreelekha, T T | |
| dc.date.accessioned | 2018-07-24T06:04:31Z | |
| dc.date.available | 2018-07-24T06:04:31Z | |
| dc.date.issued | 2017-11-15 | |
| dc.identifier.citation | Biomacromolecules,18(12):4041-4053 | en_US |
| dc.identifier.uri | http://10.10.100.66:8080/xmlui/handle/123456789/3201 | |
| dc.description.abstract | Biopolymer-capped gold nanoparticles (AuNPs) were perceived for tracing biodistribution in a solid tumor mice through surface-enhanced Raman scattering (SERS) fingerprinting. In this strategy, a robust and ecofriendly green chemistry approach was adopted to construct galactoxyloglucan (PST001) endowed AuNPs (PST-GNPs) with cancer-cell-selective toxic nature and excellent biocompatibility. Plasmonically enhanced lightscattering properties facilitated PST-GNPs to be a superior SERS substrate with high Raman signal enhancement. In this context, PST-GNPs were scrutinized for the noninvasive labelfree SERS live-cell spectral imaging to evaluate the fingerprint molecular details of cellular processes. Consequently, the inherent SERS feature of PST-GNPs enabled us to investigate the dynamic and complex nature with NP biodistrubution in tumor-bearing mice on a SERS platform that illustrated the tumor targeting nature. Henceforth, the present findings emphasized a futuristic clinically relevant scenario for tracing the in vivo NP dissemination in a label-free fashion for providing vital biochemical details on a molecular level. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | American Chemical Society | en_US |
| dc.title | Plasmonically Enhanced Galactoxyloglucan Endowed Gold Nanoparticles Exposed Tumor Targeting Biodistribution Envisaged in a Surface-Enhanced Raman Scattering Platform | en_US |
| dc.type | Article | en_US |