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https://www.researchgate.net/publication/316094627_Non-Ionic_Surfactant_Vesicles_Niosomes_as_New_Drug_Delivery_Systems
Non-Ionic Surfactant Vesicles (Niosomes) as New Drug Delivery Systems been used to enhance insulin permeability through Caco-2 cell monolayer 4-fold, compared with insulin alone (Moghassemi et al ...
https://www.mdpi.com/1999-4923/11/2/55/pdf
pharmaceutics Review Advances of Non-Ionic Surfactant Vesicles (Niosomes) and Their Application in Drug Delivery Xuemei Ge 1,†, Minyan Wei 2,†, Suna He 3 and Wei-En Yuan 2,* 1 School of Light Industry and Food Engineering, Nanjing Forestry University, Nanjing 210037, China; [email protected] 2 Engineering Research Center of Cell & Therapeutic Antibody, Ministry of …
https://www.mdpi.com/1999-4923/11/2/55/htm
Non-Ionic surfactant based vesicles, also known as niosomes, have attracted much attention in pharmaceutical fields due to their excellent behavior in encapsulating both hydrophilic and hydrophobic agents. In recent years, it has been discovered that these vesicles can improve the bioavailability of drugs, and may function as a new strategy for delivering several typical of therapeutic agents ...
http://discovery.ucl.ac.uk/1368915/
Science & Technology, Life Sciences & Biomedicine, Pharmacology & Pharmacy, non-ionic surfactants, niosomes, drug delivery, self-assembly, AMPHIPHILE-CHOLESTEROL VESICLES, MONOSTEARATE SPAN-60 NIOSOMES, ALKYL GLYCOSIDE VESICLES, CORNEUM IN-VITRO, NONIONIC SURFACTANT, STRATUM-CORNEUM, OCTYL GLUCOSIDE, SODIUM STIBOGLUCONATE, DOXORUBICIN NIOSOMES ...
https://link.springer.com/article/10.1208/s12249-017-0897-8
Non-ionic surfactant (NIS) based in situ forming vesicles (ISVs) present an affordable alternative to the traditional systems for the parenteral control of drug release. In this work, NIS based ISVs encapsulating tenoxicam were prepared using the emulsion method. Tenoxicam-loaded ISVs were prepared using a 22.31 full factorial experimental design, where three factors were evaluated as ...
https://www.deepdyve.com/lp/elsevier/non-ionic-surfactant-based-vesicles-niosomes-in-drug-delivery-DolY0FyjwR
Read "Non-ionic surfactant based vesicles (niosomes) in drug delivery, International Journal of Pharmaceutics" on DeepDyve, the largest online rental service for scholarly research with thousands of academic publications available at your fingertips.
https://www.semanticscholar.org/paper/NIOSOMES%3A-A-NOVEL-DRUG-DELIVERY-SYSTEM-Nvs-Saini/d11dbcf42919371b52342476e924891f20f531c8
Niosomes are formations of vesicles by hydrating mixture of cholesterol and nonionic surfactants. Different novel approaches used for delivering these drugs include liposomes, microspheres, nanotechnology, micro emulsions, antibody-loaded drug delivery, magnetic microcapsules, implantable pumps and niosomes.
https://link.springer.com/article/10.1007%2Fs11743-017-2023-z
Sep 26, 2017 · Nonionic surfactants are capable of forming nano-range vesicles upon self-assembling in an aqueous medium. These vesicles are highly stable, low in toxicity, and cost-effective. Owing to their ability to solubilize both hydrophilic and hydrophobic substances, they are of great interest for drug solubilization and delivery. This study describes the synthesis and characterization of two new ...
https://onlinelibrary.wiley.com/doi/abs/10.1002/jps.21944
Nonionic surfactant based vesicles (niosomes) are novel drug delivery systems formed from the self‐assembly of nonionic amphiphiles in aqueous media. In the present study niosomal formulations of Paclitaxel (PCT), an antineoplastic agent, were prepared using different surfactants (Tween 20, 60, Span 20, 40, 60, Brij 76, 78, 72) by film ...
https://www.hindawi.com/journals/bmri/2014/263604/
Abstract. With the recent advancement in the field of ocular therapy, drug delivery approaches have been elevated to a new concept in terms of nonionic surfactant vesicles (NSVs), that is, the ability to deliver the therapeutic agent to a patient in a staggered profile.
https://www.japsonline.com/admin/php/uploads/497_pdf.pdf
various advantages of vesicular systems (niosomes) to develop the effective delivery system to achieve maximum effective concentration. Niosomes, nonionic surfactant vesicles with lamellar structure which may be unilamellar and multilamellar serve to be efficient in providing these required advantages.
https://www.semanticscholar.org/paper/Characterization-of-niosomes-prepared-with-various-Bayindir-Yuksel/e581e7dd41e02d8123fa25f57f94d6ba66e3e406
Nonionic surfactant based vesicles (niosomes) are novel drug delivery systems formed from the self-assembly of nonionic amphiphiles in aqueous media. In the present study niosomal formulations of Paclitaxel (PCT), an antineoplastic agent, were prepared using different surfactants (Tween 20, 60, Span 20, 40, 60, Brij 76, 78, 72) by film hydration method. PCT was successfully entrapped in all of ...
https://www.igi-global.com/chapter/non-ionic-surfactant-vesicles-niosomes-as-new-drug-delivery-systems/174125
Non-Ionic Surfactant Vesicles (Niosomes) as New Drug Delivery Systems: 10.4018/978-1-5225-1762-7.ch007: Lipid vesicular systems composed of hydrated amphihiles with or without bilayer inducing agents such as cholesterol. On the basis of used amphiphilic molecule
https://pubs.acs.org/doi/10.1021/acs.molpharmaceut.7b00352
Small interfering RNAs (siRNA) have a broad potential as therapeutic agents to reversibly silence any target gene of interest. The clinical application of siRNA requires the use of safe and effective delivery systems. In this study, we investigated the use of nonionic surfactant vesicles (NISV) for the delivery of siRNA. Different types of NISV formulations were synthesized by microfluidic ...
http://ijpsr.com/bft-article/niosomes-in-targeted-drug-delivery-some-recent-advances/?view=fulltext
Rentel C O, Bouwstra J A, Naisbett B, Junginger H E, Niosomes as a novel peroral vaccine delivery system. International Journal of Pharmaceutics 1999; 186:161–167. Ruckmani K, Jayakar B, Ghosal S K, Nonionic surfactant vesicles (niosomes) of cytarabine hydrochloride for effective treatment of leukemias: encapsulation, storage, and in vitro ...
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