Omniphilic Polysaccharide-Based Nanocarriers for Modular Molecular Delivery in a Broad Range of Biosystems

2018 ◽  
Vol 10 (43) ◽  
pp. 36711-36720 ◽  
Author(s):  
Roi Rutenberg ◽  
Daria Galaktionova ◽  
Gilad Golden ◽  
Yael Cohen ◽  
Yael Levi-Kalisman ◽  
...  
Keyword(s):  
2007 ◽  
Vol 12 (5-6) ◽  
pp. 189-199 ◽  
Author(s):  
Jan-Olav Henck ◽  
Stephen R. Byrn

2012 ◽  
Vol 3 (1) ◽  
Author(s):  
Eisaku Kondo ◽  
Ken Saito ◽  
Yuichi Tashiro ◽  
Kaeko Kamide ◽  
Shusei Uno ◽  
...  

1998 ◽  
Vol 70 (12) ◽  
pp. 2379-2384 ◽  
Author(s):  
Y. Aoyama ◽  
Yusuke Matsuda ◽  
Jirarut Chuleeraruk ◽  
K. Nishiyama ◽  
Kazuhisa Fujimoto ◽  
...  

2019 ◽  
Vol 36 (11) ◽  
pp. 1900304 ◽  
Author(s):  
Hèctor López‐Laguna ◽  
Rita Sala ◽  
Julieta M. Sánchez ◽  
Patricia Álamo ◽  
Ugutz Unzueta ◽  
...  

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Timothy M. OʼShea ◽  
Alexander L. Wollenberg ◽  
Jae H. Kim ◽  
Yan Ao ◽  
Timothy J. Deming ◽  
...  

AbstractBiomaterials hold promise for therapeutic applications in the central nervous system (CNS). Little is known about molecular factors that determine CNS foreign body responses (FBRs) in vivo, or about how such responses influence biomaterial function. Here, we probed these factors in mice using a platform of injectable hydrogels readily modified to present interfaces with different physiochemical properties to host cells. We found that biomaterial FBRs mimic specialized multicellular CNS wound responses not present in peripheral tissues, which serve to isolate damaged neural tissue and restore barrier functions. We show that the nature and intensity of CNS FBRs are determined by definable properties that significantly influence hydrogel functions, including resorption and molecular delivery when injected into healthy brain or stroke injuries. Cationic interfaces elicit stromal cell infiltration, peripherally derived inflammation, neural damage and amyloid production. Nonionic and anionic formulations show minimal levels of these responses, which contributes to superior bioactive molecular delivery. Our results identify specific molecular mechanisms that drive FBRs in the CNS and have important implications for developing effective biomaterials for CNS applications.


2020 ◽  
Vol 5 (19) ◽  
pp. 5781-5787
Author(s):  
Kaixuan Teng ◽  
Xinglong Luan ◽  
Qi An ◽  
Yantao Zhao ◽  
Xiantong Hu ◽  
...  

2016 ◽  
Vol 146 ◽  
pp. 924-937 ◽  
Author(s):  
Bhavani Miryala ◽  
Sudhakar Godeshala ◽  
Taraka Sai Pavan Grandhi ◽  
Matthew D. Christensen ◽  
Yanqing Tian ◽  
...  

Author(s):  
Jianbo Li ◽  
Hao Lin

Electroporation is a widely applied technique to deliver active molecules into the cellular compartment, to perform tasks such as gene therapy and directed stem cell differentiation, among many others. In this technique, an electric field transiently permeabilizes the cellular membrane to facilitate molecular exchange. While the permeabilization process is relatively well understood, the transport mechanisms for molecular delivery are still under debate. In this work, the role of ion electrophoresis in electroporation-mediated molecular delivery is investigated using numerical simulation. The Nernst-Planck equations for ionic transport in the extracellular and intracellular spaces are solved, respectively, and are coupled through a permeabilization model on the membrane. For the latter, an asymptotic Smoluchowski equation system is adopted, following the work of Krassowska and co-authors. The simulation is used to investigate the delivery of calcium ions into Chinese hamster ovary cells. The results indicate that ion electrophoresis is the dominant mode of transport in the delivery of small charged molecules. Furthermore, the achievable intracellular concentration is strongly influenced by the conductivity difference between the cytoplasm and the buffer, a phenomenon known as “field-amplified sample stacking”. The results agree qualitatively with the fluorescence measurements by Gabriel and Teissie´ (1999), and suggest a new possibility to simultaneously improve cell viability and efficiency in electroporation-mediated molecular delivery.


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