scholarly journals Cyclodextrin Based Nanoparticles For Improved Solubility and Drug Delivery

2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Devashish Pandey ◽  
Vikas Singh Panwar ◽  
Himanshu Mishra ◽  
Lokesh Adhikari ◽  
Mukesh Pandey ◽  
...  

Biopharmaceutical properties (Solubility and permeability etc.) of the drugs are the major factors responsible for absorbing the drug. A huge fraction of pharmaceutical drugs belongs to classes II and IV, showing more lipophilic nature with low solubility. These drugs can be complexed with cyclodextrin for improving the biopharmaceutical properties and drug delivery. Cyclodextrin is widely utilized in pharmaceutical formulations as an associate excipient to extend stability and solubility—cyclodextrin tends to form complexes, and self-aggregation property results to form nano or micro preparations. Nano preparation of cyclodextrins can be used for drug delivery. This review deals with cyclodextrin inclusion complexes/ nanoparticles, their preparations, application, and drug delivery role.

2013 ◽  
Vol 15 (1) ◽  
pp. 177-188 ◽  
Author(s):  
Elham Khodaverdi ◽  
Farnaz Sadat Mirzazadeh Tekie ◽  
Farzin Hadizadeh ◽  
Haydar Esmaeel ◽  
Seyed Ahmad Mohajeri ◽  
...  

2006 ◽  
Vol 6 (9) ◽  
pp. 2979-2985 ◽  
Author(s):  
G. Ragno ◽  
A. Risoli ◽  
G. Ioele ◽  
E. Cione ◽  
M. De Luca

Inclusion compounds of eleven dihydropyridine drugs were formed and investigated for protection against photo-induced drug degradation. Formulations of cyclodextrins and liposomes were prepared and their photoprotective ability for the encapsulated drug was monitored. Drug photodegradation was spectrophotometrically followed during exposure of the formulations to light of a Xenon lamp. ICH guidelines for photostability testing were applied. A comparison with common pharmaceutical formulations revealed optimal protection for both formulations. The use of the liposome and cyclodextrin inclusion complexes resulted in a mean drug recovery of 77 and more then 90% respectively, after a light exposure until to 30 minutes with an intensity of 21 kJ · min−1· m−2. Lercanidipine and Manidipine only did not show a satisfactory increase of photostabilization in the studied supramolecular complexes, due to their low inclusion in both the systems.


Soft Matter ◽  
2011 ◽  
Vol 7 (2) ◽  
pp. 662-669 ◽  
Author(s):  
Gongyan Liu ◽  
Qiao Jin ◽  
Xiangsheng Liu ◽  
Liping Lv ◽  
Chaojian Chen ◽  
...  

2020 ◽  
Vol 27 (6) ◽  
pp. 919-954 ◽  
Author(s):  
Raluca Ianchis ◽  
Claudia Mihaela Ninciuleanu ◽  
Ioana Catalina Gifu ◽  
Elvira Alexandrescu ◽  
Cristina Lavinia Nistor ◽  
...  

The present review aims to summarize the research efforts undertaken in the last few years in the development and testing of hydrogel-clay nanocomposites proposed as carriers for controlled release of diverse drugs. Their advantages, disadvantages and different compositions of polymers/biopolymers with diverse types of clays, as well as their interactions are discussed. Illustrative examples of studies regarding hydrogel-clay nanocomposites are detailed in order to underline the progressive researches on hydrogel-clay-drug pharmaceutical formulations able to respond to a series of demands for the most diverse applications. Brief descriptions of the different techniques used for the characterization of the obtained complex hybrid materials such as: swelling, TGA, DSC, FTIR, XRD, mechanical, SEM, TEM and biology tests, are also included. Enlightened by the presented data, we can suppose that hydrogel-clay nanocomposites will still be a challenging subject of global assiduous researches. We can dare to dream to an efficient drug delivery platform for the treatment of multiple affection concomitantly, these being undoubtedly like ”a tree of life” bearing different kinds of fruits and leaves proper for human healing.


2020 ◽  
Vol 21 (11) ◽  
pp. 885-901
Author(s):  
Shubham Thakur ◽  
Amrinder Singh ◽  
Ritika Sharma ◽  
Rohan Aurora ◽  
Subheet Kumar Jain

Background: Surfactants are an important category of additives that are used widely in most of the formulations as solubilizers, stabilizers, and emulsifiers. Current drug delivery systems comprise of numerous synthetic surfactants (such as Cremophor EL, polysorbate 80, Transcutol-P), which are associated with several side effects though used in many formulations. Therefore, to attenuate the problems associated with conventional surfactants, a new generation of surface-active agents is obtained from the metabolites of fungi, yeast, and bacteria, which are termed as biosurfactants. Objectives: In this article, we critically analyze the different types of biosurfactants, their origin along with their chemical and physical properties, advantages, drawbacks, regulatory status, and detailed pharmaceutical applications. Methods: 243 papers were reviewed and included in this review. Results: Briefly, Biosurfactants are classified as glycolipids, rhamnolipids, sophorolipids, trehalolipids, surfactin, lipopeptides & lipoproteins, lichenysin, fatty acids, phospholipids, and polymeric biosurfactants. These are amphiphilic biomolecules with lipophilic and hydrophilic ends and are used as drug delivery vehicles (foaming, solubilizer, detergent, and emulsifier) in the pharmaceutical industry. Despite additives, they have some biological activity as well (anti-cancer, anti-viral, anti-microbial, P-gp inhibition, etc.). These biomolecules possess better safety profiles and are biocompatible, biodegradable, and specific at different temperatures. Conclusion: Biosurfactants exhibit good biomedicine and additive properties that can be used in developing novel drug delivery systems. However, more research should be driven due to the lack of comprehensive toxicity testing and high production cost which limits their use.


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