SoftNanoHybrid · Polymer-Nanoparticle co-assembly for drug targeting and release kinetics: Investigation on Structure, Morphology, Responsiveness, and Nanoparticle distribution
„Хоризонт 2020“ — Действия „Мария Склодовска-Кюри“
- Период
- 2018-07-01 → 2021-02-19
- Финансиране от ЕС
- 195 455 €
- Участници
- 1
- Схема
- MSCA-IF-EF-ST
Линиите свързват координатора с партньорите.
Накратко на български
Структурата на бактериалните мембрани се анализира чрез модели с биополимери, за да се разбере как те се сглобяват. Това помага при разработването на антибиотици с подходящи свойства за борба с бактерии, които са станали устойчиви на лекарства.
Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.
Резултати накратко
Polymer-Nanoparticle co-assembly for drug targeting and release kinetics: Investigation on Structure, Morphology, Responsiveness, and Nanoparticle distribution
The soft nanohybrids formed by the bacterial amphiphiles in water are characterised with an aim to understand their role in various bacteriological processes e.g. bioadhesion, colonisation and antimicrobial resistance. A biopolymer (lipoteichoic acid, LTA) that is pH responsive has been used as a central building unit for the model systems for self-assembly. We have successfully formed and characterised the LTA self assemblies in water and examined their adsorption at the interfaces. In the actual bacteria membrane, the LTA is adhered directly via lipid-like chains with the phospholipid membrane, and accordingly could play a major role in the structural stability and integrity of the membrane. These possibilities were checked by designing mixed vesicles from phospholipids representing the actual composition of the bacteria membrane and LTA. These structures were analysed by SANS, DLS and CryoTEM, which provided conclusions on the structural effects caused by LTA on the size and distribution of the mixed vesicles. According to National Health Services (NHS) UK, several strains of bacteria have reportedly developed resistance to many different types of antibiotics, including: MRSA (methicillin-resistant Staphylococcus aureus), Clostridium difficile and the bacteria that cause multi-drug-resistant tuberculosis. In order to encounter this challenge, the molecular interactions within bacteria membrane must be understood by detailed experimental approaches, which would presumably provide suggestions for the design and development of the antibiotics with specific structural properties to tackle the resistance caused by the bacteria. Our experiments have provided useful results in this direction and this field remains open with several unanswered questions about the physicochemical understanding of these bacteria membrane processes. The objective of the project was to understand self-assembly behaviour of soft nanohybrids. Having examined the availability and costs of a number of block copolymers with different molecular weight distribution, we have focused on mixed liposomes/vesicles and their structural transformations on interactions with lipoteichoic acid (LTA).
Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз
Цел на проекта
In recent years, co-assembly of nanoparticles (NPs) into block copolymer (BCP) aggregates is emerging as an active field of research, which considers the formation of mixed aggregates that combine synergistically the NP/BCP components to generate novel properties for advanced functional materials and applications. When NPs have been incorporated into the BCP micellar aggregates, various physical parameters e.g. distribution, the content, orientation, and localization of NPs in the polymeric matrix are extremely important, which play decisive roles in determining the characteristics and applications of the NP/BCP nanohybrid.In this proposal, we aim to investigate the morphological transformations of selected model BCP micelles in the presence of magnetic NPs of different size, shape, concentration and surface functionalization. Simultaneous encapsulation of the drug molecules controlled by the NP distribution and loading will provide critical information on the correlation of drug release with the physical parameters characterizing the polymer nanohybrids. We will also examine how the distribution of NPs within co-assembled structures is correlated with the parameters characterising the polymers and NPs. The drug release kinetics for selected nanohybrid systems will be investigated to rationalize the correlation between precise control of NPs localization/drugs loading with the drug release profile. Doxorubicin (Anti-cancer drug) containing BCP-NP nanohybrid will be formulated by solvent assisted dispersion technique. The drug release kinetics will be investigated by dialysis against tris buffer (pH 7.4/5.0) at 37oC.
Оригинален текст от CORDIS (на английски).
Участници
- UNIVERSITY OF BRISTOL · BRISTOLКоординаторОбединеното кралство
Връзки
Данни: CORDIS, © Европейски съюз
