journal article·2019-05

PEO-b-PCL grafted niosomes: The cooperativilty of amphiphilic components and their properties in vitro and in vivo

Natassa Pippa, Nikolaos Naziris, Dimitris Stellas, Christina Massala, Konstantina Zouliati, Stergios Pispas, Costas Demetzos, Aleksander Forys, Andrzej Marcinkowski, Barbara Trzebicka

Publisher page

Abstract

Niosomes belong to drug delivery systems and consist mainly of non-ionic surfactants and cholesterol. In this study, we designed and developed systems composed of non-ionic surfactants i.e. Tween 80, Span 80 and cholesterol with and without poly(ethylene oxide)-b-poly(ε-caprolactone) (PEO-b-PCL) block copolymer, using different molar ratios of the above components. The nanosystems were formed by the thin-film hydration method with purified water as dispersion medium. Several physicochemical techniques were utilized in order to study the physicochemical and morphological characteristics of the prepared assemblies. The results showed that the presence of the block copolymer alters significantly the size and morphology of neat surfactant/cholesterol niosomes. The ageing studies also revealed that the stability is strongly dependent on the nature and the molar ratios of the components. Moreover, neither of the studied nanosystems exhibited elevated signs of cellular toxicity in vitro nor acute systemic toxicity in vivo short-term experiments. This investigation covers a new field of drug delivery platforms those of niosomes composed by different biomaterials i.e. surfactants and block copolymers.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Advancements in Transdermal Drug Delivery · Surfactants and Colloidal Systems · Advanced Drug Delivery Systems

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (29)

Show source-provided references
1. Recent advances in non-ionic surfactants vesicles (niosomes): self-assembly, fabrication, characterization, drug delivery applications and limitations10.3109/10717544.2013.838077 ↗
2. Nano-niosomes as nanoscale drug delivery systems: an illustrated review10.1016/j.jconrel.2014.04.015 ↗
3. Niosomes from 80s to present: the state of the art10.1016/j.cis.2013.11.018 ↗
4. Formulation and in vitro assessment of minoxidil niosomes for enhanced skin delivery10.1016/j.ijpharm.2009.04.020 ↗
5. Niosomes: a controlled and novel drug delivery system10.1248/bpb.34.945 ↗
6. Development of a topical niosomal preparation of acetazolamide: preparation and evaluation10.1211/0022357044896 ↗
7. Preparation and evaluation of reverse-phase evaporation and multilamellar niosomes as ophthalmic carriers of acetazolamide10.1016/j.ijpharm.2005.09.023 ↗
8. Preparation and characterization of pripylthiouracil niosomes10.1080/08982100600992542 ↗
9. A review on novel vesicular drug delivery: proniosomes10.3109/10717544.2013.841783 ↗
10. Effect of some formulation parameters on flurbiprofen encapsulation and release rates of niosomes prepared from proniosomes10.1016/j.ijpharm.2008.05.031 ↗
11. Polymeric modification and its implication in drug delivery: poly-ε-caprolactone (PCL) as a model polymer10.1021/mp3001952 ↗
12. Biodegradable poly(epsilon-caprolactone)-poly(ethylene glycol) copolymers as drug delivery system10.1016/j.ijpharm.2009.07.033 ↗
13. PEG-PCL-based nanomedicines: a biodegradable drug delivery system and its application10.1016/j.jconrel.2017.05.028 ↗
14. Thermosensitive porphyrin-incorporated hydrogel with four-arm PEG-PCL copolymer (II):doxorubicin loaded hydrogel as a dual fluorescent drug delivery system for simultaneous imaging tracking in vivo10.1080/10717544.2017.1289570 ↗
15. PCL-based thermo-gelling polymers for in vivo delivery of chemotherapeutics to tumors10.1016/j.msec.2017.02.005 ↗
16. PEO-b-PCL:DPPC chimeric nanocarriers: self-assembly aspects in aqueous and biological media and drug incorporation10.1039/c3sm27447k ↗
17. The imaging and the fractal metrology if chimeric liposomal drug delivery nano systems: the role of macromolecular architecture of polymeric guest10.3109/08982104.2014.891232 ↗
18. PEO-b-PCL grafted DPPC liposomes: physicochemical characterization and stability studies of novel bio-inspired advanced drug delivery nano systems (aDDnSs)10.1166/jnn.2014.8869 ↗
19. In vitro evaluation of pH-sensitive polymer/niosome complexes10.1021/bm010036z ↗
20. Polymer based pH-sensitive carriers as a means to improve the cytoplasmic delivery of drugs10.1016/S0378-5173(02)00183-7 ↗
21. Anti-inflammatory activity of gel containing novel elastic niosomes entrapped with diclofenac diethylammonium10.1016/j.ijpharm.2008.04.033 ↗
22. Physicochemical properties and skin permeation of Span 60/Tween 60 niosomes of ellagic acid10.1016/j.ijpharm.2011.11.032 ↗
23. Phase separation and nanodomain formation in hybrid polymer/lipid vesicles10.1021/mz500748f ↗
24. Morphological diversity of block copolymer/lipid chimeric nanostructures10.1007/s11051-017-4021-5 ↗
25. Cryo transmission electron microscopy of liposomes and related structures10.1016/S0927-7757(00)00516-1 ↗
26. Imaging of liposomes by transmission electron microscopy10.1007/978-1-4939-7352-1_8 ↗
27. Measurement and interpretation of electrokinetic phenomena10.1016/j.jcis.2006.12.075 ↗
28. In vitro characterization of Span 65 niosomal formulations containing proteins10.2174/1567201812666150511095432 ↗
29. Chimeric lipid/block copolymer nanovesicles: physico-chemical and bio-compatibility evaluation10.1016/j.ejpb.2016.08.003 ↗