PMID- 35547883 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20220516 IS - 2046-2069 (Electronic) IS - 2046-2069 (Linking) VI - 8 IP - 62 DP - 2018 Oct 15 TI - Enhanced distance-dependent fluorescence quenching using size tuneable core shell silica nanoparticles. PG - 35840-35848 LID - 10.1039/c8ra05929b [doi] AB - Silica nanoparticles (SNPs) have been used as favoured platforms for sensor, drug delivery and biological imaging applications, due to their ease of synthesis, size-control and bespoke physico-chemical properties. In this study, we have developed a protocol for the synthesis of size-tuneable SNPs, with diameters ranging from 20 nm to 500 nm, through the optimisation of experimental components required for nanoparticle synthesis. This protocol was also used to prepare fluorescent SNPs, via covalent linkages of fluorophores, to the nanoparticle matrix using 3-aminopropyltriethoxysilane (APTES). This enabled the fabrication of ratiometric, fluorescent, pH-sensitive nanosensors (75 nm diameter) composed SNPs covalently linked to two pH-sensitive fluorescent dyes Oregon Green (OG) and 5(6)-carboxyfluorescein (FAM) and a reference fluorescent dye 5-(6)-carboxytetramethylrhodamine (TAMRA), extending the dynamic range of measurement from pH 3.5 to 7.5. In addition, size-tuneable, core-shell SNPs, covalently linked to a fluorescent TAMRA core were synthesised to investigate distance-dependant fluorescence quenching between TAMRA and black hole quencher 2 (BHQ2(R)) using nanometre-sized silica shells as physical spacers. The results showed a significant fluorescence quenching could be observed over greater distances than that reported for the classical distance-dependent molecular fluorescence quenching techniques, e.g. the Forster (fluorescence) resonance energy transfer (FRET). The methods and protocols we have detailed in this manuscript will provide the basis for the reproducible production of size tunable SNPs, which will find broad utility in the development of sensors for biological applications. CI - This journal is (c) The Royal Society of Chemistry. FAU - Elsutohy, Mohamed M AU - Elsutohy MM AUID- ORCID: 0000-0002-6771-9226 AD - Boots Science Building, School of Pharmacy, University Park Campus, University of Nottingham Nottingham NG7 2RD UK jon.aylott@nottingham.ac.uk. AD - Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Al-Azhar University Assiut 71524 Egypt. FAU - Selo, Amjad AU - Selo A AD - Boots Science Building, School of Pharmacy, University Park Campus, University of Nottingham Nottingham NG7 2RD UK jon.aylott@nottingham.ac.uk. FAU - Chauhan, Veeren M AU - Chauhan VM AUID- ORCID: 0000-0002-2067-4630 AD - Boots Science Building, School of Pharmacy, University Park Campus, University of Nottingham Nottingham NG7 2RD UK jon.aylott@nottingham.ac.uk. FAU - Tendler, Saul J B AU - Tendler SJB AD - Boots Science Building, School of Pharmacy, University Park Campus, University of Nottingham Nottingham NG7 2RD UK jon.aylott@nottingham.ac.uk. AD - Vice-Chancellor's Department, University of York Heslington York YO10 5DD UK. FAU - Aylott, Jonathan W AU - Aylott JW AD - Boots Science Building, School of Pharmacy, University Park Campus, University of Nottingham Nottingham NG7 2RD UK jon.aylott@nottingham.ac.uk. LA - eng PT - Journal Article DEP - 20181019 PL - England TA - RSC Adv JT - RSC advances JID - 101581657 PMC - PMC9088216 COIS- The authors declare no conflict of interest. EDAT- 2018/10/19 00:00 MHDA- 2018/10/19 00:01 PMCR- 2018/10/19 CRDT- 2022/05/13 11:19 PHST- 2018/07/11 00:00 [received] PHST- 2018/10/06 00:00 [accepted] PHST- 2022/05/13 11:19 [entrez] PHST- 2018/10/19 00:00 [pubmed] PHST- 2018/10/19 00:01 [medline] PHST- 2018/10/19 00:00 [pmc-release] AID - c8ra05929b [pii] AID - 10.1039/c8ra05929b [doi] PST - epublish SO - RSC Adv. 2018 Oct 19;8(62):35840-35848. doi: 10.1039/c8ra05929b. eCollection 2018 Oct 15.