Multifunctional System with Camptothecin and [12]aneN<sub>3</sub> Units for Effective <i>In Vivo</i> Anti Pancreatic Cancer through Synergistic Chemotherapy, Gene Therapy, and Photodynamic Therapy

Maximizing drug cargo carrying capacity in blood circulation, controlling the <i>in vivo</i> fate of nanoparticles, and precisely drug release to tumor targets are the main aims of multifunctional nanomedicine-based antitumor therapy. Here we combined macrocyclic polyamine di(triazole-[12]aneN<sub>3</sub>) (<b>M</b>) and chemical drug camptothecin (CPT, <b>C</b>) through photosensitizer 1,1-dicyano-2-phenyl-2-(4-diphenylamino) phenyl-ethylene (<b>DT</b>) containing the cleavable disulfide (<b>S</b>) linkage as an all-in-one theranostic nanoprodrug, <b>MDTSC</b>. The corresponding compound with carbon chain (<b>C</b>) linkage, <b>MDTCC</b>, was also prepared for a comparison study. <b>MDTSC</b> showed the ability to carry plasmids, including the p53 tumor suppressor gene, to form lipoplexes with a size of ∼150 nm. Further addition of DOPE-PEG<sub>2k</sub> resulted in the hybrid lipoplexes <b>MDTSC</b>/DOPE-PEG<sub>2k</sub>@DNA, which showed good stability in blood circulation and good biocompatibility to normal cell lines. Experiments demonstrated that the hybrid lipoplexes were able to realize the successful cellular uptake and endosomal escape, to generate ROS under visible light irradiation as well as to trigger the localized release of CPT and the plasmid encoding p53 in tumor cells. <i>In vitro</i>, the hybrid lipoplexes showed better EGFP expression than the commercial Lipo2000, and markedly reduced tumor cell proliferation and migration rate irrespective of whether the BxPC-3 cell lines were grown on plates or 3D tumor spheroids. <i>In vivo</i>, the hybrid lipoplexes showed effective anticancer activity by reducing the BxPC-3 pancreatic tumor growth by 99% through the synergetic combination of chemotherapy, photodynamic therapy, and gene therapy. This research represented the first example of using a cocktail of three therapeutic approaches to achieve cooperative and effective anti pancreatic cancer treatment <i>in vivo</i> and <i>in vitro</i>.

Authors

Institutions

Publication Details

Journal
ACS Applied Materials & Interfaces
Published
2024-11-25
DOI
https://doi.org/10.1021/acsami.4c12936
Citations
3
Primary Topic
Nanoplatforms for cancer theranostics
Type
article
Field-Weighted Citation Impact
0.55

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Multifunctional System with Camptothecin and [12]aneN3 Units for Effective In Vivo Anti Pancreatic Cancer through Synergistic Chemotherapy, Gene Therapy, and Photodynamic Therapy

Zi‐Han Zhang, De-Zhong Xu, Zhong‐Lin Lu, Rui Liu et al.
3 citations
ACS Applied Materials & Interfaces
Nanoplatforms for cancer theranostics
0.55
article

Multifunctional System with Camptothecin and [12]aneN3 Units for Effective In Vivo Anti Pancreatic Cancer through Synergistic Chemotherapy, Gene Therapy, and Photodynamic Therapy

Zi‐Han Zhang, De-Zhong Xu, Zhong‐Lin Lu, Rui Liu, Yang Liu, Jingbo Yang, Zhi-Xuan Ren, Xi Zhang
article en
3 citations

Abstract

Maximizing drug cargo carrying capacity in blood circulation, controlling the <i>in vivo</i> fate of nanoparticles, and precisely drug release to tumor targets are the main aims of multifunctional nanomedicine-based antitumor therapy. Here we combined macrocyclic polyamine di(triazole-[12]aneN<sub>3</sub>) (<b>M</b>) and chemical drug camptothecin (CPT, <b>C</b>) through photosensitizer 1,1-dicyano-2-phenyl-2-(4-diphenylamino) phenyl-ethylene (<b>DT</b>) containing the cleavable disulfide (<b>S</b>) linkage as an all-in-one theranostic nanoprodrug, <b>MDTSC</b>. The corresponding compound with carbon chain (<b>C</b>) linkage, <b>MDTCC</b>, was also prepared for a comparison study. <b>MDTSC</b> showed the ability to carry plasmids, including the p53 tumor suppressor gene, to form lipoplexes with a size of ∼150 nm. Further addition of DOPE-PEG<sub>2k</sub> resulted in the hybrid lipoplexes <b>MDTSC</b>/DOPE-PEG<sub>2k</sub>@DNA, which showed good stability in blood circulation and good biocompatibility to normal cell lines. Experiments demonstrated that the hybrid lipoplexes were able to realize the successful cellular uptake and endosomal escape, to generate ROS under visible light irradiation as well as to trigger the localized release of CPT and the plasmid encoding p53 in tumor cells. <i>In vitro</i>, the hybrid lipoplexes showed better EGFP expression than the commercial Lipo2000, and markedly reduced tumor cell proliferation and migration rate irrespective of whether the BxPC-3 cell lines were grown on plates or 3D tumor spheroids. <i>In vivo</i>, the hybrid lipoplexes showed effective anticancer activity by reducing the BxPC-3 pancreatic tumor growth by 99% through the synergetic combination of chemotherapy, photodynamic therapy, and gene therapy. This research represented the first example of using a cocktail of three therapeutic approaches to achieve cooperative and effective anti pancreatic cancer treatment <i>in vivo</i> and <i>in vitro</i>.

ACS Applied Materials & InterfacesVol. 16(49)
Ministry of Education of the People's Republic of China (CN), Beijing Normal University (CN), National Institutes for Food and Drug Control (CN)
National Natural Science Foundation of China, Beijing Municipal Natural Science Foundation
Openalex Percentile: Top 36%
Nanoplatforms for cancer theranostics
0.55
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.