ナノメディシンとナノテクノロジーのジャーナル

概要

Determine Tumor Site-Dependent Transport Properties Delivery of Nanotherapeutics and Their Efficacy

Pranav Shende

Therapeutic effectiveness of anticancer medicines delivered systemically may be hampered by insufficient distribution of the medications to tumours. Can create therapeutic resistance based on drug delivery. PEGylated liposomal doxorubicin (PLD), for example, uses an increased permeability and retention effect to preferentially accumulate in tumours. Their clinical results and anticancer effects, however, vary widely amongst tumour types and are minimal. We looked into whether the tumour site affected the quantity and effectiveness of PLD delivered to tumours. We created mouse breast models with orthotopic primary tumours or liver metastases. Utilising 4 T1 cells for cancer PLD effectively treated cancers that developed in primary mammary tissue. but not in the liver, locations. We discovered that variations in treatment effectiveness were not caused by the intrinsic biological defence mechanisms in cancer cells but rather were linked to variations in transport characteristics that depended on the tumour site, such as the amount of PLD delivered, blood vessel function, relative vascular permeability, and mechanical pressure in tumours. As a result, site-dependent transport features in tumours can be employed as phenotypic surrogate markers for tumour drug delivery and therapeutic effectiveness.