4.8 Article

Aptamer and Peptide-Engineered Polydopamine Nanospheres for Target Delivery and Tumor Perfusion in Synergistic Chemo-Phototherapy of Pancreatic Cancer

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 15, Issue 13, Pages 16539-16551

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.3c01967

Keywords

pancreatic cancer; chemo-phototherapy; desmoplastic stroma; tumor perfusion; controllable release

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Pancreatic cancer is a leading cause of cancer death with low survival rates. Chemotherapy is often used, but the tumor's stroma can hinder drug delivery and lead to chemoresistance. In this study, a novel approach using targeted nanoparticles loaded with chemotherapy drugs was developed for synergistic chemo-phototherapy against pancreatic cancer. The nanoparticles effectively enhanced drug delivery and killing effects.
Pancreatic cancer (PC) is the fourth leading cause of cancer death, and the 5 year survival rate is only 4%. Chemotherapy is the treatment option for the majority of PC patients diagnosed at an advanced stage, whereas the desmoplastic stroma of PC could block the perfusion of chemotherapeutic agents to tumor tissues and contribute generally to chemoresistance. Therefore, the clinical status of PC calls for an urgent exploration in the effective treatment strategy. Chemo-phototherapy is an emerging modality against malignant tumors, but owing to the low targeting ability of theranostic agents or unspecific accumulation in the tumor region, majority of chemophototherapy techniques have disappointing therapeutic efficiencies. Herein, we have explored CD71-specific targeting aptamers and paclitaxel (PTX)-modified polydopamine (PDA) nanospheres with the conjugation of peptidomimetic AV3 (termed Apt-PDA@PTX/AV3 bioconjugates) to specifically target and combat PC in vivo by synergistic chemo-phototherapy. After the delivery of nanotheranostic agents to the tumor microenvironment (TME) or subsequent endocytic uptake by PC cells, a simultaneous release of AV3 and PTX from Apt-PDA@PTX/AV3 bioconjugates via near-infrared (NIR) irradiation can decrease desmoplastic stroma to enhance tumor perfusion and tumor-killing effects. Meanwhile, PDA cores utilize NIR laser to create unendurable hyperthermia within TME to cook tumors. Taken together, the current study finally suggests that our Apt-PDA@PTX/AV3 bioconjugates could act as a novel therapeutic approach by synergistic chemophototherapy for the inhibition of PC.

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