Rong Ni

Dr. Rong Ni

orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2006 in Journal of the American Chemical Society
Verified
Journal Article
Closed access
YZYuri Zimenkov
Yuri Zimenkov
SDSteven N. Dublin
Steven N. Dublin
RNRong Ni
Rong Ni
RTRaymond S. Tu
Raymond S. Tu
VBVictor Breedveld
Victor Breedveld
VCVincent P. Conticello
Vincent P. Conticello

12 November 2014 in Journal of the American Chemical Society
Verified
Journal Article
Closed access
RNRong Ni
Rong Ni
YCYing Chau
Ying Chau

14 October 2014 in Journal of the American Chemical Society
Verified
Journal Article
Closed access
CLChen Liang
Chen Liang
RNRong Ni
Rong Ni
JSJillian Smith
Jillian Smith
WCW. Seth Childers
W. Seth Childers
AMAnil Mehta
Anil Mehta
DLDavid G. Lynn
David G. Lynn

1 November 2016 in Advanced Drug Delivery Reviews
Verified
Journal Article
Closed access
RNRong Ni
Rong Ni
JZJunli Zhou
Junli Zhou
NHNaushad Hossain
Naushad Hossain
YCYing Chau
Ying Chau

26 May 2010 in Angewandte Chemie International Edition
Verified
Journal Article
Closed access
PDF file
WCW. Seth Childers
W. Seth Childers
AMAnil Mehta
Anil Mehta
RNRong Ni
Rong Ni
JTJeannette V. Taylor
Jeannette V. Taylor
DLDavid G. Lynn
David G. Lynn

9 July 2019 in Life
Verified
Journal Article
Open access
PDF file
RNRong Ni
Rong Ni
RFRuilu Feng
Ruilu Feng
YCYing Chau
Ying Chau
The discovery of the genetic roots of various human diseases has motivated the exploration of different exogenous nucleic acids as therapeutic agents to treat these genetic disorders (inherited or acquired). However, the physicochemical properties of nucleic acids render them liable to degradation and also restrict their cellular entrance and gene translation/inhibition at the correct cellular location. Therefore, gene condensation/protection and guided intracellular trafficking are necessary for exogenous nucleic acids to function inside cells. Diversified cationic formulation materials, including natural and synthetic lipids, polymers, and proteins/peptides, have been developed to facilitate the intracellular transportation of exogenous nucleic acids. The chemical properties of different formulation materials determine their special features for nucleic acid delivery, so understanding the property–function correlation of the formulation materials will inspire the development of next-generation gene delivery carriers. Therefore, in this review, we focus on the chemical properties of different types of formulation materials and discuss how these formulation materials function as protectors and cellular pathfinders for nucleic acids, bringing them to their destination by overcoming different cellular barriers.