Capsules Based on Lipid Vesicles: Potentiality for Drug Delivery

2012 ◽  
pp. 165-180
Keyword(s):  
Nanoscale ◽  
2014 ◽  
Vol 6 (13) ◽  
pp. 7635 ◽  
Author(s):  
Sheng Wang ◽  
Hanjie Wang ◽  
Zhongyun Liu ◽  
Liangliang Wang ◽  
Xiaomin Wang ◽  
...  

2010 ◽  
Vol 16 (4) ◽  
pp. 456-461 ◽  
Author(s):  
Valentina Bello ◽  
Giovanni Mattei ◽  
Paolo Mazzoldi ◽  
Nicoletta Vivenza ◽  
Paolo Gasco ◽  
...  

AbstractLipid-containing nanostructures, in the form of solid lipid nanoparticles or iron oxide nanoparticles (NPs) coated with a lipid shell, were used as case studies for assessing and optimizing staining for transmission electron microscopy structural and compositional characterization. These systems are of paramount importance as drug delivery systems or as bio-compatible contrast agents. In particular, we have treated the systems with a negative (phospshotungstic acid) or with a positive (osmium tetroxide) staining agent. For iron-oxide NPs coated with the lipid shell, negative staining was more efficient with respect to the positive one. Nevertheless, in particular cases the combination of the two staining procedures provided more complete morphological and compositional characterization of the particles.


2016 ◽  
Vol 12 ◽  
pp. 1-8
Author(s):  
S. Nagalakshmi ◽  
T. Sandeep ◽  
S. Shanmuganathan

Delivery of drug through topical route, delivers most convenient and novel approach. The Skin can offer several advantages as a route of drug administration although its barrier nature makes it difficult for most drugs to penetrate in to and permeate through it. During the past decades there has been a lot of interest in lipid vesicles as a tool to improve topical drug delivery. Vesicular system such as liposomes, niosomes, ethosomes and elastic deformable vesicles provide an alternative for improved skin drug delivery. In fact vesicles can act as drug carriers controlling drug release. The Research findings were intended to develop sustained release of aceclofenac niosomes formulations in order to reduce gastrointestinal disturbances and to provide better effect when applied topically. Niosomes of aceclofenac was prepared by modified ether injection method using different ratio of surfactants (Tween 20, 40, 60 & 80) with cholesterol and drug. The developed formulations were optimized based on the high entrapment efficiency and in-vitro release studies. Optimized batch was selected and made in to topical niosomal gel using gelling agents like carbopol and sodium carboxy methyl cellulose. Formulation were evaluated for various parameters like vesicle shape, vesicle size, entrapment efficiency, drug content, compatibility studies, in-vitro release studies and stability studies. Ether injection method was found to be most satisfactory in terms of niosome particle size, drug entrapment efficiency was found to be 88.68 ±0.64 % and in-vitro release studies showed 40% of sustain drug release at the end of 8 hrs of study when compared with marketed formulation. Hence, the formulated niosomal topical gel was found to be a better alternative when compared to the marketed formulation in terms of better efficacy, bioavailability and permeation.


2016 ◽  
Vol 11 (6) ◽  
pp. 1-15
Author(s):  
Akhilesh Dubey ◽  
Prabhakara Prabhu ◽  
Jasmine Patel ◽  
Srinivas Hebbar ◽  
C Shastry ◽  
...  

2017 ◽  
pp. 154-184
Author(s):  
Abbas Pardakhty

Lipid vesicular systems composed of hydrated amphihiles with or without bilayer inducing agents such as cholesterol. On the basis of used amphiphilic molecule different nomenclature are used as liposomes, ufasomes and niosomes. Nonionic surfactants with mono-, di- or trialkyl chains form niosomes which are lipid vesicles with more chemical stability in comparison with phospholipids of liposomes. Both hydrophobic and hydrophilic chemicals can be encapsulated in niosomes as a new drug delivery system. This drug carrier system could have administered via injection, oral, pulmonary, vaginal, rectal, ophthalmic, nasal or transdermal routes with penetration enhancing potential. This chapter presents a detailed explain about niosome forming components, methods of preparation and routes of administration. Many examples for drug delivery potential of niosomes are also available in this review. Vaccine adjuvant and genetic substances vector capabilities are not given here.


Author(s):  
Abbas Pardakhty

Lipid vesicular systems composed of hydrated amphihiles with or without bilayer inducing agents such as cholesterol. On the basis of used amphiphilic molecule different nomenclature are used as liposomes, ufasomes and niosomes. Nonionic surfactants with mono-, di- or trialkyl chains form niosomes which are lipid vesicles with more chemical stability in comparison with phospholipids of liposomes. Both hydrophobic and hydrophilic chemicals can be encapsulated in niosomes as a new drug delivery system. This drug carrier system could have administered via injection, oral, pulmonary, vaginal, rectal, ophthalmic, nasal or transdermal routes with penetration enhancing potential. This chapter presents a detailed explain about niosome forming components, methods of preparation and routes of administration. Many examples for drug delivery potential of niosomes are also available in this review. Vaccine adjuvant and genetic substances vector capabilities are not given here.


2003 ◽  
Vol 774 ◽  
Author(s):  
David Needham

AbstractOur approach to biologically inspired materials and materials systems recognizes biology (at all scale levels) as a series of products that fulfill particular functions. It then links material composition and structure to function through properties and therefore attempts to bring mechanism to processes and functions of biology. As an example of this approach we have focused on the lipid bilayer membranes of blood cells, like erythrocytes and neutrophils, as a bioinspired material system for drug delivery leading to the creation of waxy, nano capsules called liposomes that can be triggered to release their drug by hyperthermia. Thus, while Nature's encapsulation technology provides the inspiration, the mechanism of drug release is non-natural. The necessary design parameters for the required functions of drug encapsulation, i.e. drug retention, circulation half life, and eventual thermally-triggered drug release, were obtained through extensive experimentation and modeling of artificial lipid vesicles by us and others, with much of the mechanical and thermomechanical properties, molecular exchange, and in vitro performance investigated by a direct micropipet manipulation technique. With respect to cancer chemotherapy, the unmet need for primary solid tumors is to deliver more drug to the tumor tissue thereby reducing the tumor size (debulking) while at the same time reducing toxic side effects. It is with these criteria in mind that we developed the temperature-triggered liposome for the treatment of solid tumors. This paper then, describes this liposome development and its performance in vivo, where, in some cases, the temperature-triggered release of drug directly in the blood stream and tumor resulted in complete tumor regression. What this example also shows is that through material property measurement and modeling, new insights into Nature's functions and designs can be discovered in a reverse engineering process from which new products can then be forward engineered to solve engineering and product problems in health, technology, and the environment.


Author(s):  
Munmun Bardhan ◽  
Anupa Majumdar ◽  
Sayantan Jana ◽  
Tapas Ghosh ◽  
Uttam Pal ◽  
...  

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