Hierarchical self-assembled nanostructures of lactone-derived thiobarbiturate homopolymers for stimuli-responsive delivery applications. Issue 19 (29th April 2020)
- Record Type:
- Journal Article
- Title:
- Hierarchical self-assembled nanostructures of lactone-derived thiobarbiturate homopolymers for stimuli-responsive delivery applications. Issue 19 (29th April 2020)
- Main Title:
- Hierarchical self-assembled nanostructures of lactone-derived thiobarbiturate homopolymers for stimuli-responsive delivery applications
- Authors:
- Mandal, Piyali
Patra, Diptendu
Shunmugam, Raja - Abstract:
- Abstract : Hierarchical self-assembled nanostructures of lactone-derived thiobarbiturate homopolymers for stimuli-responsive delivery applications are shown. Abstract : The synthesis of unique amphiphilic biodegradable molecular architectures from polylactone (polycaprolactone, polylactide)-derived thiobarbiturate homopolymers (TBA-PCL-PCAP, TBA-PLA-PCAP ) and their characterization are described. Here, the lactones provided hydrophobicity, and the barbiturate provided hydrophilicity. To produce the compounds, Friedel–Crafts acylation and ring-opening polymerization (ROP ) techniques were applied. The identities of the products were confirmed using 1 H-NMR, 13 C-NMR, and FT-IR spectroscopic techniques. These newly designed homopolymers self-assembled in aqueous solutions. Dynamic light scattering (DLS ) and critical aggregation concentration (CAC ) studies were carried out to confirm the formation of aggregates in solution. To investigate the morphologies of these homopolymers, transmission electron microscopy (TEM ) and cryo-TEM studies were performed and they confirmed the formation of hierarchical superstructures. This unique amphiphilicity-induced homopolymer self-assembly was demonstrated for the first time for lactone-based polymers. First, the encapsulation of hydrophobic (Nile red) dye was done to prove the concept, and then the drug doxorubicin was investigated. A study of the dependence of the release of the drug on pH indicated the stimulus responsiveness of theseAbstract : Hierarchical self-assembled nanostructures of lactone-derived thiobarbiturate homopolymers for stimuli-responsive delivery applications are shown. Abstract : The synthesis of unique amphiphilic biodegradable molecular architectures from polylactone (polycaprolactone, polylactide)-derived thiobarbiturate homopolymers (TBA-PCL-PCAP, TBA-PLA-PCAP ) and their characterization are described. Here, the lactones provided hydrophobicity, and the barbiturate provided hydrophilicity. To produce the compounds, Friedel–Crafts acylation and ring-opening polymerization (ROP ) techniques were applied. The identities of the products were confirmed using 1 H-NMR, 13 C-NMR, and FT-IR spectroscopic techniques. These newly designed homopolymers self-assembled in aqueous solutions. Dynamic light scattering (DLS ) and critical aggregation concentration (CAC ) studies were carried out to confirm the formation of aggregates in solution. To investigate the morphologies of these homopolymers, transmission electron microscopy (TEM ) and cryo-TEM studies were performed and they confirmed the formation of hierarchical superstructures. This unique amphiphilicity-induced homopolymer self-assembly was demonstrated for the first time for lactone-based polymers. First, the encapsulation of hydrophobic (Nile red) dye was done to prove the concept, and then the drug doxorubicin was investigated. A study of the dependence of the release of the drug on pH indicated the stimulus responsiveness of these innovative nanostructures. Analysis of the results revealed that, irrespective of the backbone, the barbiturate moiety was responsible for the self-assembled nanoaggregates and the related fascinating properties. … (more)
- Is Part Of:
- Polymer chemistry. Volume 11:Issue 19(2020)
- Journal:
- Polymer chemistry
- Issue:
- Volume 11:Issue 19(2020)
- Issue Display:
- Volume 11, Issue 19 (2020)
- Year:
- 2020
- Volume:
- 11
- Issue:
- 19
- Issue Sort Value:
- 2020-0011-0019-0000
- Page Start:
- 3340
- Page End:
- 3348
- Publication Date:
- 2020-04-29
- Subjects:
- Polymers -- Periodicals
Macromolecules -- Periodicals
Polymerization -- Periodicals
547.705 - Journal URLs:
- http://www.rsc.org/Publishing/Journals/PY/Index.asp ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d0py00367k ↗
- Languages:
- English
- ISSNs:
- 1759-9954
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6547.703400
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 13885.xml