Bioactive Natural Small Molecule-Tuned Coassembly of Photosensitive Drugs for Highly Efficient Synergistic and Enhanced Type I Photochemotherapy.
Animals
Antineoplastic Agents
/ chemistry
Cell Line, Tumor
Cell Proliferation
/ drug effects
Cell Survival
/ drug effects
Chlorophyllides
Density Functional Theory
Drug Carriers
/ chemistry
Drug Screening Assays, Antitumor
Humans
Injections, Intravenous
Mammary Neoplasms, Experimental
/ drug therapy
Mice
Molecular Dynamics Simulation
Molecular Structure
Oleanolic Acid
/ administration & dosage
Particle Size
Photochemotherapy
Photosensitizing Agents
/ chemistry
Porphyrins
/ administration & dosage
Surface Properties
coassembly
drug delivery
natural small molecules
photodynamic therapy
synergistic therapy
Journal
ACS applied materials & interfaces
ISSN: 1944-8252
Titre abrégé: ACS Appl Mater Interfaces
Pays: United States
ID NLM: 101504991
Informations de publication
Date de publication:
30 Sep 2020
30 Sep 2020
Historique:
pubmed:
2
9
2020
medline:
11
3
2021
entrez:
2
9
2020
Statut:
ppublish
Résumé
Self-assembling natural small molecules (NSMs) with favorable anticancer activity are of increasing interest as novel drug delivery platforms without structural modification for biomedical applications. However, a lack of knowledge and practicability of NSMs as drug carriers limited their current biomedical application. Here, via a green and facile supramolecular coassembly strategy, we report and develop a series of carrier-free terpenoid natural small molecule-mediated coassembled photosensitive drugs for enhanced and synergistic chemo/photodynamic therapy. After screening 17 terpenoid NSMs, we identified 11 compounds that could form coassembled NSMs-Ce6 NPs with regulatable drug sizes. Analysis of the representative betulonic acid (BC)-mediated nano-coassemblies (BC-Ce6 NPs) reveals the high efficiency of the coassembly strategy and highlights the tremendous potential of NSMs as novel drug delivery platforms. Through molecular dynamics simulation and theoretical calculations, we elucidate the mystery of the coassembly process, indicating that the linear coplanar arrangement of BC dimeric units is primarily responsible for the formation of rod-like or spherical morphology. Meanwhile, we demonstrated that the reduced energy gap between the singlet and triplet excited states (Δ
Identifiants
pubmed: 32870657
doi: 10.1021/acsami.0c13164
doi:
Substances chimiques
Antineoplastic Agents
0
Chlorophyllides
0
Drug Carriers
0
Photosensitizing Agents
0
Porphyrins
0
betulonic acid
0
phytochlorin
5S2CCF3T1Z
Oleanolic Acid
6SMK8R7TGJ
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM