Liposomal drug delivery systems: from concept to clinical applications.
By Theresa M. Allen, P. Cullis. Advanced Drug Delivery Reviews, 2013
4,362 citations recorded by the source corpus.
Subfields: Biomaterials, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/b8bb9bdebf669c6ac9ea5b0954696f96646e07cf
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Biomaterials
In Molecular Biology
Citations in the corpus
- The Smart Drug Delivery System and Its Clinical Potential (2016, background): “Although recent research and reviews have developed and summarized several novel aspects for nanomaterials that being used as smart drug carriers [1-6], few of them have been finally translated into clinics for real-world applications [7-9].”
- Current Trends and Challenges in the Clinical Translation of Nanoparticulate Nanomedicines: Pathways for Translational Development and Commercialization (2018, background): “Potential reasons for this discrepancy have previously been reviewed (Sawant and Torchilin, 2012; Allen and Cullis, 2013), and include factors such as target accessibility and expression, disease-dependent anatomical and physiological barriers, and formulation stability.”
- Engineering the Delivery System for CRISPR-based Genome Editing (2018, background): “Lipid-based drug carriers have been FDA-approved for small molecule delivery since the 1980s [42].”
- Smart nanoparticles for cancer therapy (2023, background): “49 Smart liposomes that have been functionally changed are also sensitive to a variety of internal and external stimuli, such as enzyme transformations, pH changes, redox reactions, microwaves, ultrasound, and light.”
- Liposomes: structure, composition, types, and clinical applications (2022, background): “Liposomes' active targeting increases the selectivity of liposome interaction with diseased cells and triggers receptor-mediated endocytosis of the liposome and its payload into the desired cellular target [101, 102].”