Epidermal Growth Factor-Conjugated Poly(ethylene glycol)-block- Poly(δ-valerolactone) Copolymer Micelles for Targeted Delivery of Chemotherapeutics

2006 ◽  
Vol 17 (2) ◽  
pp. 399-409 ◽  
Author(s):  
Faquan Zeng ◽  
Helen Lee ◽  
Christine Allen
RSC Advances ◽  
2015 ◽  
Vol 5 (26) ◽  
pp. 20025-20034 ◽  
Author(s):  
Yuling Li ◽  
Sai Wang ◽  
Dandan Zhu ◽  
Yuling Shen ◽  
Baixiang Du ◽  
...  

Reversibly shell cross-linked micelles based on a lipoic acid (LA) decorated triblock copolymer poly(ethylene glycol)-b-poly(γ-benzyl-l-glutamate)-b-poly(l-phenylalanine) have been developed for efficient intracellular delivery of DOX.


2013 ◽  
Vol 49 (1) ◽  
pp. 429-435 ◽  
Author(s):  
Boris. P. Nikolaev ◽  
Yaroslav Yu Marchenko ◽  
Liudmila Yu Yakovleva ◽  
Tatiana M. Zimina ◽  
Alexei V. Soloviev ◽  
...  

Biomaterials ◽  
2015 ◽  
Vol 72 ◽  
pp. 112-124 ◽  
Author(s):  
Jacob L. Roam ◽  
Ying Yan ◽  
Peter K. Nguyen ◽  
Ian S. Kinstlinger ◽  
Michael K. Leuchter ◽  
...  

Pharmaceutics ◽  
2020 ◽  
Vol 12 (11) ◽  
pp. 1068 ◽  
Author(s):  
Danijela Zukancic ◽  
Estelle J. A. Suys ◽  
Emily H. Pilkington ◽  
Azizah Algarni ◽  
Hareth Al-Wassiti ◽  
...  

Targeted delivery of nucleic acids to lymph nodes is critical for the development of effective vaccines and immunotherapies. However, it remains challenging to achieve selective lymph node delivery. Current gene delivery systems target mainly to the liver and typically exhibit off-target transfection at various tissues. Here we report novel lipid nanoparticles (LNPs) that can deliver plasmid DNA (pDNA) to a draining lymph node, thereby significantly enhancing transfection at this target organ, and substantially reducing gene expression at the intramuscular injection site (muscle). In particular, we discovered that LNPs stabilized by 3% Tween 20, a surfactant with a branched poly(ethylene glycol) (PEG) chain linking to a short lipid tail, achieved highly specific transfection at the lymph node. This was in contrast to conventional LNPs stabilized with a linear PEG chain and two saturated lipid tails (PEG-DSPE) that predominately transfected at the injection site (muscle). Interestingly, replacing Tween 20 with Tween 80, which has a longer unsaturated lipid tail, led to a much lower transfection efficiency. Our work demonstrates the importance of PEGylation in selective organ targeting of nanoparticles, provides new insights into the structure–property relationship of LNPs, and offers a novel, simple, and practical PEGylation technology to prepare the next generation of safe and effective vaccines against viruses or tumours.


2001 ◽  
Vol 77 (1-2) ◽  
pp. 27-38 ◽  
Author(s):  
Yuji Yamamoto ◽  
Yukio Nagasaki ◽  
Yukio Kato ◽  
Yuichi Sugiyama ◽  
Kazunori Kataoka

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