» Articles » PMID: 37242560

Drug Delivery Strategies for the Treatment of Pancreatic Cancer

Overview
Journal Pharmaceutics
Publisher MDPI
Date 2023 May 27
PMID 37242560
Authors
Affiliations
Soon will be listed here.
Abstract

Pancreatic cancer is fast becoming a global menace and it is projected to be the second leading cause of cancer-related death by 2030. Pancreatic adenocarcinomas, which develop in the pancreas' exocrine region, are the predominant type of pancreatic cancer, representing about 95% of total pancreatic tumors. The malignancy progresses asymptomatically, making early diagnosis difficult. It is characterized by excessive production of fibrotic stroma known as desmoplasia, which aids tumor growth and metastatic spread by remodeling the extracellular matrix and releasing tumor growth factors. For decades, immense efforts have been harnessed toward developing more effective drug delivery systems for pancreatic cancer treatment leveraging nanotechnology, immunotherapy, drug conjugates, and combinations of these approaches. However, despite the reported preclinical success of these approaches, no substantial progress has been made clinically and the prognosis for pancreatic cancer is worsening. This review provides insights into challenges associated with the delivery of therapeutics for pancreatic cancer treatment and discusses drug delivery strategies to minimize adverse effects associated with current chemotherapy options and to improve the efficiency of drug treatment.

Citing Articles

Informatics strategies for early detection and risk mitigation in pancreatic cancer patients.

Jin D, Khan N, Gu W, Lei H, Goel A, Chen T Neoplasia. 2025; 60:101129.

PMID: 39842383 PMC: 11763847. DOI: 10.1016/j.neo.2025.101129.


Temoporfin-Conjugated PEGylated Poly(,-dimethylacrylamide)-Coated Upconversion Colloid for NIR-Induced Photodynamic Therapy of Pancreatic Cancer.

Shapoval O, Patsula V, Vetvicka D, Engstova H, Oleksa V, Kabesova M Biomacromolecules. 2024; 25(9):5771-5785.

PMID: 38888278 PMC: 11388470. DOI: 10.1021/acs.biomac.4c00317.


Targeted Nanoparticle-Based Diagnostic and Treatment Options for Pancreatic Cancer.

Gu X, Minko T Cancers (Basel). 2024; 16(8).

PMID: 38672671 PMC: 11048786. DOI: 10.3390/cancers16081589.


Design, Synthesis, and Antitumor Evaluation of an Opioid Growth Factor Bioconjugate Targeting Pancreatic Ductal Adenocarcinoma.

Budka J, Debowski D, Mai S, Narajczyk M, Hac S, Rolka K Pharmaceutics. 2024; 16(2).

PMID: 38399336 PMC: 10892429. DOI: 10.3390/pharmaceutics16020283.

References
1.
Xie Q, Jia L, Liu Y, Wei C . Synergetic anticancer effect of combined gemcitabine and photodynamic therapy on pancreatic cancer in vivo. World J Gastroenterol. 2009; 15(6):737-41. PMC: 2653444. DOI: 10.3748/wjg.15.737. View

2.
Cun X, Chen J, Li M, He X, Tang X, Guo R . Tumor-Associated Fibroblast-Targeted Regulation and Deep Tumor Delivery of Chemotherapeutic Drugs with a Multifunctional Size-Switchable Nanoparticle. ACS Appl Mater Interfaces. 2019; 11(43):39545-39559. DOI: 10.1021/acsami.9b13957. View

3.
Carvalho T, Di Molfetta D, Greco M, Koltai T, Alfarouk K, Reshkin S . Tumor Microenvironment Features and Chemoresistance in Pancreatic Ductal Adenocarcinoma: Insights into Targeting Physicochemical Barriers and Metabolism as Therapeutic Approaches. Cancers (Basel). 2021; 13(23). PMC: 8657427. DOI: 10.3390/cancers13236135. View

4.
Hafeez U, Parakh S, Gan H, Scott A . Antibody-Drug Conjugates for Cancer Therapy. Molecules. 2020; 25(20). PMC: 7587605. DOI: 10.3390/molecules25204764. View

5.
Nishigaki T, Takahashi T, Serada S, Fujimoto M, Ohkawara T, Hara H . Anti-glypican-1 antibody-drug conjugate is a potential therapy against pancreatic cancer. Br J Cancer. 2020; 122(9):1333-1341. PMC: 7189381. DOI: 10.1038/s41416-020-0781-2. View