scholarly journals Immunoliposome-mediated drug delivery to Plasmodium -infected and non-infected red blood cells as a dual therapeutic/prophylactic antimalarial strategy

2015 ◽  
Vol 210 ◽  
pp. 217-229 ◽  
Author(s):  
Ernest Moles ◽  
Patricia Urbán ◽  
María Belén Jiménez-Díaz ◽  
Sara Viera-Morilla ◽  
Iñigo Angulo-Barturen ◽  
...  
Author(s):  
Mauro Magnani ◽  
Luigia Rossi ◽  
Anna Casabianca ◽  
Alessandra Fraternale ◽  
Giuditta Schiavano ◽  
...  

2019 ◽  
Vol 48 (1) ◽  
pp. 236-246 ◽  
Author(s):  
Monica Piergiovanni ◽  
Giustina Casagrande ◽  
Francesca Taverna ◽  
Ilaria Corridori ◽  
Marta Frigerio ◽  
...  

1995 ◽  
Vol 03 (02) ◽  
pp. 447-455
Author(s):  
FORTUNATA SOLIMANO

A mathematical model for the drug delivery to macrophages of the tissues by using a preassigned cohort of red blood cells loaded with a drug is presented. This model is a system of three nonlinear differential equations, with a discrete time delay and an input depending on the time. The input should be controlled in order to obtain the longest duration of the therapeutic effect.


Small Methods ◽  
2017 ◽  
Vol 1 (12) ◽  
pp. 1700270 ◽  
Author(s):  
Junjie Yan ◽  
Jicheng Yu ◽  
Chao Wang ◽  
Zhen Gu

Pharmaceutics ◽  
2020 ◽  
Vol 12 (5) ◽  
pp. 440 ◽  
Author(s):  
Patrick M. Glassman ◽  
Carlos H. Villa ◽  
Anvay Ukidve ◽  
Zongmin Zhao ◽  
Paige Smith ◽  
...  

Red blood cells (RBC) have great potential as drug delivery systems, capable of producing unprecedented changes in pharmacokinetics, pharmacodynamics, and immunogenicity. Despite this great potential and nearly 50 years of research, it is only recently that RBC-mediated drug delivery has begun to move out of the academic lab and into industrial drug development. RBC loading with drugs can be performed in several ways—either via encapsulation within the RBC or surface coupling, and either ex vivo or in vivo—depending on the intended application. In this review, we briefly summarize currently used technologies for RBC loading/coupling with an eye on how pharmacokinetics is impacted. Additionally, we provide a detailed description of key ADME (absorption, distribution, metabolism, elimination) changes that would be expected for RBC-associated drugs and address unique features of RBC pharmacokinetics. As thorough understanding of pharmacokinetics is critical in successful translation to the clinic, we expect that this review will provide a jumping off point for further investigations into this area.


2004 ◽  
Vol 31 (2) ◽  
pp. 92-101 ◽  
Author(s):  
S. Serafini ◽  
L. Rossi ◽  
A. Antonelli ◽  
A. Fraternale ◽  
A. Cerasi ◽  
...  

IUBMB Life ◽  
2011 ◽  
Vol 63 (8) ◽  
pp. 621-631 ◽  
Author(s):  
Sara Biagiotti ◽  
Maria Filomena Paoletti ◽  
Alessandra Fraternale ◽  
Luigia Rossi ◽  
Mauro Magnani

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