The current clinical management of PC is discussed, as well as recent advances in nanomedicine‐based IP delivery, which address important challenges to be overcome towards designing optimal nanocarriers for IP therapy in vivo.
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This article is published in Advanced Drug Delivery Reviews.The article was published on 2017-01-01 and is currently open access. It has received 66 citations till now.
TL;DR: The aim of the present review is to highlight and discuss recent advances made in the last years on the design of chemical and physical HA-based hydrogels and their application for biomedical purposes, in particular, drug delivery.
TL;DR: Data is presented that a local IP delivery of a miRNA/siRNA combination holds the potential to improve pancreatic cancer therapy and shows improved therapeutic effect when compared with individual therapies.
TL;DR: This work proposes a new magnetically assisted strategy to elevate drug penetration into peritoneal tumor nodules and improve IP chemotherapy and shows an order of magnitude increase in the final intratumoral concentration of drug-coated MNPs with respect to free cytotoxic agents.
TL;DR: Bidirectional chemotherapy combining XELOX with PIPAC with cisplatin and doxororubicin is well tolerated, can induce objective tumor regression and is associated with a promising survival in PMGC.
TL;DR: Targeting of p32 with linTT1 tumor‐penetrating peptide improves tumor selectivity and antitumor efficacy of IP pro‐apoptotic NWs, and may represent a general strategy to increase their therapeutic index.
TL;DR: Tumor ascites fluids from guinea pigs, hamsters, and mice contain activity that rapidly increases microvascular permeability, and this activity is secreted by these tumor cells and a variety of other tumor cell lines in vitro.
TL;DR: There are now unprecedented opportunities to understand and overcome drug resistance through the clinical assessment of rational therapeutic drug combinations and the use of predictive biomarkers to enable patient stratification.
TL;DR: Lipidic nanoparticles are the first nanomedicine delivery system to make the transition from concept to clinical application, and they are now an established technology platform with considerable clinical acceptance.
TL;DR: This review presents why PLGA has been chosen to design nanoparticles as drug delivery systems in various biomedical applications such as vaccination, cancer, inflammation and other diseases.
TL;DR: In this paper, the authors proposed a passive targeting mechanism, active targeting strategies using ligands or antibodies directed against selected tumor targets amplify the specificity of these therapeutic nanoparticles, enabling them to carry their loaded active drugs to cancer cells by selectively using the unique pathophysiology of tumors.
This item is the archived peer‐reviewed author‐version of: Nanomedicine‐based intraperitoneal therapy for the treatment of peritoneal carcinomatosis – Mission possible ?