Formulation and Evaluation of Anti-Arthritis Drug Loaded Stealth Liposomes

2021 ◽  
Vol 14 (3) ◽  
pp. 1313-1318
Author(s):  
Jerin Annie Thomas ◽  
Shajan Abraham ◽  
Steffy P Raju ◽  
Christina Das ◽  
Anu Abraham ◽  
...  
Keyword(s):  
2021 ◽  
pp. 1-13
Author(s):  
Khushboo Katharotiya ◽  
Gajanan Shinde ◽  
Dhaval Katharotiya ◽  
Santosh Shelke ◽  
Rakesh Patel ◽  
...  

2012 ◽  
Vol 8 (7) ◽  
pp. 1152-1161 ◽  
Author(s):  
Wenbing Dai ◽  
Tingyuan Yang ◽  
Yiguang Wang ◽  
Xueqing Wang ◽  
Jiancheng Wang ◽  
...  

2019 ◽  
Vol 19 (11) ◽  
pp. 6899-6906 ◽  
Author(s):  
Salma E. Ahmed ◽  
Hesham G. Moussa ◽  
Ana M. Martins ◽  
Yassmine Abbas ◽  
Mohammad H. Al-Sayah ◽  
...  

Typical methods used in cancer treatment, including chemotherapy, are debilitating because of the various adverse side effects experienced by cancer patients. The free drug injected into the patient at given doses affects both healthy and cancerous cells. Therefore, novel methods are being researched to ensure the selectivity of the treatment. The purpose of this study is to test the release of a model fluorescent drug, calcein, from echogenic stealth liposomes, triggered by lowfrequency pulsed ultrasound. Several experimental parameters related to the ultrasound (US) and the investigated liposomes were varied in order to examine their effect on the acoustic release. Upon analysis of experimental results, the study concluded that release can be maximized by optimizing the sonication frequency, power density, and US pulse duration. When a non-isothermal chamber is used to conduct the experiments, it is important to have longer ‘Off’ than ‘On’ US periods in order to avoid overheating the liposomes. Applying such pulsation pattern can also be utilized to achieve slower release rates, which safely meet the desired drug levels at the end of the session. Our study also concluded that optimizing the liposome concentration is vital to delivering desired drug doses. Additionally, the type of lipids used in the synthesis should be carefully selected to produce stable yet acoustically sensitive liposomes capable of releasing at desired rates.


2020 ◽  
Vol 590 ◽  
pp. 119955
Author(s):  
Maryam Tabassum Hussain ◽  
Mattia Tiboni ◽  
Yvonne Perrie ◽  
Luca Casettari
Keyword(s):  

2020 ◽  
Vol 2020 ◽  
pp. 1-31
Author(s):  
Antonio Vassallo ◽  
Maria Francesca Silletti ◽  
Immacolata Faraone ◽  
Luigi Milella

Today’s human society, product of decades of progress in all fields of knowledge, would have been unimaginable without the discovery of antibiotics and more generally of antimicrobials. However, from the beginning, the scientific community was aware that microorganisms through various strategies were able to hinder and render vain antibiotic action. Common examples are the phenomena of persistence, tolerance, and resistance, up to the creation of the feared bacterial biofilms. Antibiotics are a precious but equally labile resource that must be preserved but at the same time reinforced to safeguard their effectiveness. Nanoparticulate systems such as nanobactericides, with their inherent antibacterial activity, and nanocarriers, which operate as drug delivery systems for conventional antibiotics, are innovative therapies made available by nanotechnology. Inorganic nanoparticles are effective both as nanobactericides (AgNPs, ZnONPs, and TiO2NPs) and as nanocarriers (AgNPs, AuNPs, ZnONPs, and TiO2NPs) against sensitive and multi-drug-resistant bacterial strains. Liposomes are among the most studied and flexible antibiotic delivery platforms: conventional liposomes allow passive targeting at the mononuclear phagocytic system (MPS); “stealth” liposomes prevent macrophage uptake so as to eradicate infections in tissues and organs outside MPS; thanks to their positive charge, cationic liposomes interact preferentially with bacterial and biofilm surfaces, acting as innate antibacterials as well as drug delivery systems (DDS); fusogenic liposomes have fluid bilayers that promote fusion with microbial membranes; and finally, ligand-targeted liposomes provide active targeting at infection sites. Dendrimers are among the most recent and attractive nanoparticulate systems, thanks to their multibranched nanoarchitecture, which equipped them with multiple active sites for loading antibiotics and also interacting with bacteria. Finally, nanoantibiotics represent a new hopeful generation of antibiotic candidates capable of increasing or even restoring the clinical efficacy of “old” antibiotics rendered useless by the resistance phenomena.


2012 ◽  
Vol 45 (12) ◽  
pp. 746-749 ◽  
Author(s):  
E. A. Kotova ◽  
A. P. Polozkova ◽  
T. V. Denisova ◽  
I. I. Krasnyuk ◽  
N. A. Oborotova

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