MRI monitoring of intratumoral drug delivery and prediction of the therapeutic effect with a multifunctional thermosensitive liposome

Biomaterials ◽  
2011 ◽  
Vol 32 (27) ◽  
pp. 6570-6578 ◽  
Author(s):  
Tatsuaki Tagami ◽  
Warren D. Foltz ◽  
Mark J. Ernsting ◽  
Carol M. Lee ◽  
Ian F. Tannock ◽  
...  
2013 ◽  
Vol 2013 ◽  
pp. 1-13 ◽  
Author(s):  
Wenbo Zhan ◽  
Xiao Yun Xu

The effectiveness of anticancer treatments is often hampered by the serious side effects owing to toxicity of anticancer drugs and their undesirable uptake by healthy cells in vivo. Thermosensitive liposome-mediated drug delivery has been developed as part of research efforts aimed at improving therapeutic efficacy while reducing the associated side effect. Since multiple steps are involved in the transport of drug-loaded liposomes, drug release, and its uptake, mathematical models become an indispensible tool to analyse the transport processes and predict the outcome of anticancer treatment. In this study, a computational model is developed which incorporates the key physical and biochemical processes involved in drug delivery and cellular uptake. The model has been applied to idealized tumour geometry, and comparisons are made between continuous infusion of doxorubicin and thermosensitive liposome-mediated delivery. Results show that thermosensitive liposome-mediated delivery performs better in reducing drug concentration in normal tissues, which may help lower the risk of associated side effects. Compared with direct infusion over a 2-hour period, thermosensitive liposome delivery leads to a much higher peak intracellular concentration of doxorubicin, which may increase cell killing in tumour thereby enhancing the therapeutic effect of the drug.


Author(s):  
Ana C. Marques ◽  
Paulo J. Costa ◽  
Sérgia Velho ◽  
Maria H. Amaral

Nanoscale ◽  
2020 ◽  
Vol 12 (46) ◽  
pp. 23838-23850
Author(s):  
Giulia Brachi ◽  
Javier Ruiz-Ramírez ◽  
Prashant Dogra ◽  
Zhihui Wang ◽  
Vittorio Cristini ◽  
...  

Intratumoral drug delivery is a promising approach for the treatment of glioblastoma multiforme (GBM).


2019 ◽  
Vol 3 (6) ◽  
pp. 1159-1167 ◽  
Author(s):  
Yuxun Ding ◽  
Jinjian Liu ◽  
Xue Li ◽  
Linlin Xu ◽  
Chang Li ◽  
...  

pH-Reduction dual responsive nanocarriers (DRNs) achieve programmable release of CA4 and CDDP in cancer therapy.


Nanoscale ◽  
2019 ◽  
Vol 11 (32) ◽  
pp. 15057-15071 ◽  
Author(s):  
Di Shi ◽  
Gujie Mi ◽  
Yan Shen ◽  
Thomas J. Webster

With the combination of thermosensitive liposome and an external AMF, SPIONs inside the liposome can therefore transform the electromagnetic energy to heat and trigger drug release at desired temperature.


Pharmaceutics ◽  
2019 ◽  
Vol 11 (9) ◽  
pp. 460 ◽  
Author(s):  
Eliana B. Souto ◽  
João Dias-Ferreira ◽  
Ana López-Machado ◽  
Miren Ettcheto ◽  
Amanda Cano ◽  
...  

The eye presents extensive perspectives and challenges for drug delivery, mainly because of the extraordinary capacity, intrinsic to this path, for drugs to permeate into the main circulatory system and also for the restrictions of the ocular barriers. Depending on the target segment of the eye, anterior or posterior, the specifications are different. The ocular route experienced in the last decades a lot of progresses related with the development of new drugs, improved formulations, specific-designed delivery and even new routes to administer a drug. Concomitantly, new categories of materials were developed and adapted to encapsulate drugs. With such advances, a multiplicity of parameters became possible to be optimized as the increase in bioavailability and decreased toxic effects of medicines. Also, the formulations were capable to easily adhere to specific tissues, increase the duration of the therapeutic effect and even target the delivery of the treatment. The ascending of new delivery systems for ocular targeting is a current focus, mainly because of the capacity to extend the normal time during which the drug exerts its therapeutic effect and, so, supplying the patients with a product which gives them fewer side effects, fewer number of applications and even more effective outcomes to their pathologies, surpassing the traditionally-used eye drops. Depending on the systems, some are capable of increasing the duration of the drug action as gels, emulsions, prodrugs, liposomes, and ocular inserts with hydrophilic properties, improving the absorption by the cornea. In parallel, other devices use as a strategy the capacity to sustain the release of the carried drugs by means of erodible and non-erodible matrices. This review discusses the different types of advanced formulations used for ocular delivery of therapeutics presenting the most recent patents according to the clinical applications.


RSC Advances ◽  
2019 ◽  
Vol 9 (63) ◽  
pp. 37067-37078
Author(s):  
Xiaoyan Tan ◽  
Yanlin Zhou ◽  
Li Shen ◽  
Han Jia ◽  
Xiaorong Tan

For mitochondria-targeted nano-drug delivery systems against cancer, effectively targeting and releasing the drug into mitochondria are the keys to improve the therapeutic effect.


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.


Sign in / Sign up

Export Citation Format

Share Document