Laura McKay, Natali Joma, Dusica Maysinger and Ashok Kakkar
{"title":"含苯并[c]杂蒽荧光团的软纳米颗粒:易于合成和比例pH传感。","authors":"Laura McKay, Natali Joma, Dusica Maysinger and Ashok Kakkar","doi":"10.1039/D5TB01322D","DOIUrl":null,"url":null,"abstract":"<p >Polymeric nanoparticles offer considerable potential in resolving key issues related to the delivery of small lipophilic pharmaceutics. However, significant challenges remain with respect to the development and application of multifunctional, easily accessible fluorescent tools for tracing the cellular uptake and trafficking of soft nanoparticles. We have evaluated a platform for this purpose utilizing the pH-responsive molecular sensor seminaphthofluorescein-C (benzo[<em>c</em>]xanthene ‘SNAFL-C’); its chemical conjugation to an asymmetric miktoarm star polymer (AB<small><sub>2</sub></small>) at its hydrophobic arm terminus; and traceable polymeric nanoparticles through self-assembly of SNAFL-AB<small><sub>2</sub></small> or physical encapsulation of the fluorophore. The characteristic high Stokes shift and ratiometric emission behaviour of SNAFL-C were retained in its polymer conjugate as well as in the self-assembled structures. Assemblies of the miktoarm fluorophore conjugate exhibited moderately reduced brightness as a result of aggregation induced quenching, an effect not observed for the physically encapsulated species. Fluorescence quenching experiments probing the partitioning of SNAFL-C in the core shell structures revealed localization of the primary fluorescent species in equilibrium based on their physiochemical properties, providing rationalization of differing aggregation behaviour observed for physically encapsulated and covalently linked formulations. Live cell fluorescence imaging in human glioblastoma cells integrating both SNAFL-C and its nanoformulations demonstrated the utility of the fluorophore in biological imaging applications and highlighted the necessity of detailed and stepwise spectral and photophysical evaluations. Collectively, these systems offer new avenues to explore fluorescence imaging using polymeric nanocarriers, leading to insights of broad importance to drug delivery and theragnostics.</p>","PeriodicalId":83,"journal":{"name":"Journal of Materials Chemistry B","volume":" 37","pages":" 11790-11808"},"PeriodicalIF":6.1000,"publicationDate":"2025-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/tb/d5tb01322d?page=search","citationCount":"0","resultStr":"{\"title\":\"Soft nanoparticles incorporating a benzo[c]xanthene fluorophore: facile synthesis and ratiometric pH sensing\",\"authors\":\"Laura McKay, Natali Joma, Dusica Maysinger and Ashok Kakkar\",\"doi\":\"10.1039/D5TB01322D\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Polymeric nanoparticles offer considerable potential in resolving key issues related to the delivery of small lipophilic pharmaceutics. However, significant challenges remain with respect to the development and application of multifunctional, easily accessible fluorescent tools for tracing the cellular uptake and trafficking of soft nanoparticles. We have evaluated a platform for this purpose utilizing the pH-responsive molecular sensor seminaphthofluorescein-C (benzo[<em>c</em>]xanthene ‘SNAFL-C’); its chemical conjugation to an asymmetric miktoarm star polymer (AB<small><sub>2</sub></small>) at its hydrophobic arm terminus; and traceable polymeric nanoparticles through self-assembly of SNAFL-AB<small><sub>2</sub></small> or physical encapsulation of the fluorophore. The characteristic high Stokes shift and ratiometric emission behaviour of SNAFL-C were retained in its polymer conjugate as well as in the self-assembled structures. Assemblies of the miktoarm fluorophore conjugate exhibited moderately reduced brightness as a result of aggregation induced quenching, an effect not observed for the physically encapsulated species. Fluorescence quenching experiments probing the partitioning of SNAFL-C in the core shell structures revealed localization of the primary fluorescent species in equilibrium based on their physiochemical properties, providing rationalization of differing aggregation behaviour observed for physically encapsulated and covalently linked formulations. Live cell fluorescence imaging in human glioblastoma cells integrating both SNAFL-C and its nanoformulations demonstrated the utility of the fluorophore in biological imaging applications and highlighted the necessity of detailed and stepwise spectral and photophysical evaluations. 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Soft nanoparticles incorporating a benzo[c]xanthene fluorophore: facile synthesis and ratiometric pH sensing
Polymeric nanoparticles offer considerable potential in resolving key issues related to the delivery of small lipophilic pharmaceutics. However, significant challenges remain with respect to the development and application of multifunctional, easily accessible fluorescent tools for tracing the cellular uptake and trafficking of soft nanoparticles. We have evaluated a platform for this purpose utilizing the pH-responsive molecular sensor seminaphthofluorescein-C (benzo[c]xanthene ‘SNAFL-C’); its chemical conjugation to an asymmetric miktoarm star polymer (AB2) at its hydrophobic arm terminus; and traceable polymeric nanoparticles through self-assembly of SNAFL-AB2 or physical encapsulation of the fluorophore. The characteristic high Stokes shift and ratiometric emission behaviour of SNAFL-C were retained in its polymer conjugate as well as in the self-assembled structures. Assemblies of the miktoarm fluorophore conjugate exhibited moderately reduced brightness as a result of aggregation induced quenching, an effect not observed for the physically encapsulated species. Fluorescence quenching experiments probing the partitioning of SNAFL-C in the core shell structures revealed localization of the primary fluorescent species in equilibrium based on their physiochemical properties, providing rationalization of differing aggregation behaviour observed for physically encapsulated and covalently linked formulations. Live cell fluorescence imaging in human glioblastoma cells integrating both SNAFL-C and its nanoformulations demonstrated the utility of the fluorophore in biological imaging applications and highlighted the necessity of detailed and stepwise spectral and photophysical evaluations. Collectively, these systems offer new avenues to explore fluorescence imaging using polymeric nanocarriers, leading to insights of broad importance to drug delivery and theragnostics.
期刊介绍:
Journal of Materials Chemistry A, B & C cover high quality studies across all fields of materials chemistry. The journals focus on those theoretical or experimental studies that report new understanding, applications, properties and synthesis of materials. Journal of Materials Chemistry A, B & C are separated by the intended application of the material studied. Broadly, applications in energy and sustainability are of interest to Journal of Materials Chemistry A, applications in biology and medicine are of interest to Journal of Materials Chemistry B, and applications in optical, magnetic and electronic devices are of interest to Journal of Materials Chemistry C.Journal of Materials Chemistry B is a Transformative Journal and Plan S compliant. Example topic areas within the scope of Journal of Materials Chemistry B are listed below. This list is neither exhaustive nor exclusive:
Antifouling coatings
Biocompatible materials
Bioelectronics
Bioimaging
Biomimetics
Biomineralisation
Bionics
Biosensors
Diagnostics
Drug delivery
Gene delivery
Immunobiology
Nanomedicine
Regenerative medicine & Tissue engineering
Scaffolds
Soft robotics
Stem cells
Therapeutic devices