Academic literature on the topic 'Lipid-core polymeric nanoparticles'

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Lipid-core polymeric nanoparticles.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Lipid-core polymeric nanoparticles"

1

ZHANG, LI, and LIANGFANG ZHANG. "LIPID–POLYMER HYBRID NANOPARTICLES: SYNTHESIS, CHARACTERIZATION AND APPLICATIONS." Nano LIFE 01, no. 01n02 (2010): 163–73. http://dx.doi.org/10.1142/s179398441000016x.

Full text
Abstract:
Nanotechnology has been extensively explored in the past decade to develop a myriad of functional nanostructures to facilitate the delivery of therapeutic and imaging agents for various medical applications. Liposomes and polymeric nanoparticles represent two primary delivery vehicles that are currently under investigation. While many advantages of these two particle platforms have been disclosed, some intrinsic limitations remain to limit their applications at certain extent. Recently, a new type of nanoparticle platform, named lipid–polymer hybrid nanoparticle, has been developed that combin
APA, Harvard, Vancouver, ISO, and other styles
2

Islam, Mohammad Ariful, Emma K. G. Reesor, Yingjie Xu, Harshal R. Zope, Bruce R. Zetter, and Jinjun Shi. "Biomaterials for mRNA delivery." Biomaterials Science 3, no. 12 (2015): 1519–33. http://dx.doi.org/10.1039/c5bm00198f.

Full text
Abstract:
Schematic representation of various biomaterial-based systems for mRNA delivery: (a) protamine–mRNA complex; (b) lipid nanoparticle; (c) lipid nanoparticle with inorganic compounds (e.g.apatite); (d) cationic polymeric nanoparticle; (e) lipid–polymer hybrid nanoparticles including (i) mRNA–polymer complex core surrounded by a lipid shell and (ii) polymer core surrounded by a lipid shell with mRNA absorbed onto the surface; and (f) gold nanoparticle.
APA, Harvard, Vancouver, ISO, and other styles
3

Yu, Deng-Guang, Kenneth White, Nicholas Chatterton, Ying Li, Lingling Li, and Xia Wang. "Structural lipid nanoparticles self-assembled from electrospun core–shell polymeric nanocomposites." RSC Advances 5, no. 13 (2015): 9462–66. http://dx.doi.org/10.1039/c4ra14001j.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Patel, Ravi R., Gayasuddin Khan, Sundeep Chaurasia, Nagendra Kumar, and Brahmeshwar Mishra. "Rationally developed core–shell polymeric-lipid hybrid nanoparticles as a delivery vehicle for cromolyn sodium: implications of lipid envelop on in vitro and in vivo behaviour of nanoparticles upon oral administration." RSC Advances 5, no. 93 (2015): 76491–506. http://dx.doi.org/10.1039/c5ra12732g.

Full text
Abstract:
In the present study, cromolyn sodium, a highly water soluble molecule was encapsulated into rationally designed, core–shell polymeric-lipid hybrid nanoparticles for enhancing its oral bioavailability, by improving its intestinal permeability.
APA, Harvard, Vancouver, ISO, and other styles
5

Raman, Subashini, Syed Mahmood, and Azizur Rahman. "A Review on Lipid- Polymer Hybrid Nanoparticles and Preparation with Recent Update." Materials Science Forum 981 (March 2020): 322–27. http://dx.doi.org/10.4028/www.scientific.net/msf.981.322.

Full text
Abstract:
Ongoing progression in nanotechnology has demonstrated that nanoparticles have indicated promising potential as in delivering the drug. The acceptance of nanoparticles and their applications also reported in clinical advancement to upgrade and improve the pharmacokinetic and pharmacodynamics properties of therapeutic compounds. In this review, we talk about the next-generation core-shell nanostructures like lipid-polymer hybrid nanoparticles (LHNPs) and their application and formulation aspects. Conceptually, derived from both polymeric nanoparticles and liposome, which gave them a name of hyb
APA, Harvard, Vancouver, ISO, and other styles
6

Bou, Sophie, Xinyue Wang, Nicolas Anton, Redouane Bouchaala, Andrey S. Klymchenko, and Mayeul Collot. "Lipid-core/polymer-shell hybrid nanoparticles: synthesis and characterization by fluorescence labeling and electrophoresis." Soft Matter 16, no. 17 (2020): 4173–81. http://dx.doi.org/10.1039/d0sm00077a.

Full text
Abstract:
New hybrid nanoparticles have been obtained by simple nanoprecipitation using fluorescent labeling of both the oily core (BODIPY) and the polymeric shell (rhodamine) thus allowing the use of electrophoresis to assess their formation and stability.
APA, Harvard, Vancouver, ISO, and other styles
7

Sun, Jiashu, Lu Zhang, Jiuling Wang, et al. "Tunable Rigidity of (Polymeric Core)-(Lipid Shell) Nanoparticles for Regulated Cellular Uptake." Advanced Materials 27, no. 8 (2014): 1402–7. http://dx.doi.org/10.1002/adma.201404788.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Sivadasan, Durgaramani, Muhammad Hadi Sultan, Osama Madkhali, Yosif Almoshari, and Neelaveni Thangavel. "Polymeric Lipid Hybrid Nanoparticles (PLNs) as Emerging Drug Delivery Platform—A Comprehensive Review of Their Properties, Preparation Methods, and Therapeutic Applications." Pharmaceutics 13, no. 8 (2021): 1291. http://dx.doi.org/10.3390/pharmaceutics13081291.

Full text
Abstract:
Polymeric lipid hybrid nanoparticles (PLNs) are core–shell nanoparticles made up of a polymeric kernel and lipid/lipid–PEG shells that have the physical stability and biocompatibility of both polymeric nanoparticles and liposomes. PLNs have emerged as a highly potent and promising nanocarrier for a variety of biomedical uses, including drug delivery and biomedical imaging, owing to recent developments in nanomedicine. In contrast with other forms of drug delivery systems, PLNs have been regarded as seamless and stable because they are simple to prepare and exhibit excellent stability. Natural,
APA, Harvard, Vancouver, ISO, and other styles
9

ZHENG, MINGBIN, PING GONG, DONGXUE JIA, CUIFANG ZHENG, YIFAN MA, and LINTAO CAI. "PLGA–LECITHIN–PEG CORE-SHELL NANOPARTICLES FOR CANCER TARGETED THERAPY." Nano LIFE 02, no. 01 (2012): 1250002. http://dx.doi.org/10.1142/s1793984411000359.

Full text
Abstract:
We reported the development of multifunctional poly (lactic-co-glycolic acid) (PLGA)-lecithin-polyethylene glycol (PEG) core-shell nanoparticles (NPs) that combined the beneficial properties of liposome and polymeric NPs for chemotherapeutics delivery. The particle size, surface charge and surface functional groups were easily tunable in highly reproducible manner by various formulation parameters such as lipid/polymer, 1, 2-distearoyl-sn-glycero-3-phosphoethanolamine (DSPE)-PEG- COOH /lecithin, DSPE-PEG- COOH /DSPE-PEG- NH2 mass ratio and modification of terminal groups of DSPE-PEG. We encaps
APA, Harvard, Vancouver, ISO, and other styles
10

You, Jian, Jun Zhao, Xiaoxia Wen, et al. "Chemoradiation therapy using cyclopamine-loaded liquid–lipid nanoparticles and lutetium-177-labeled core-crosslinked polymeric micelles." Journal of Controlled Release 202 (March 2015): 40–48. http://dx.doi.org/10.1016/j.jconrel.2015.01.031.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Lipid-core polymeric nanoparticles"

1

Lopes, Clarissa Elize. "DESENVOLVIMENTO E CARACTERIZAÇÃO DE NANOPARTÍCULAS LIPÍDICAS CONTENDO HALCINONIDA PARA MODULAÇÃO DA INFLAMAÇÃO NO PROCESSO DE CICATRIZAÇÃO DE LESÕES CUTÂNEAS." UNIVERSIDADE ESTADUAL DE PONTA GROSSA, 2015. http://tede2.uepg.br/jspui/handle/prefix/95.

Full text
Abstract:
Made available in DSpace on 2017-07-21T14:13:05Z (GMT). No. of bitstreams: 1 Clarissa Elize.pdf: 4457240 bytes, checksum: d8f2520757eb456c2ae4c01f7a1f0343 (MD5) Previous issue date: 2015-12-21<br>Coordenação de Aperfeiçoamento de Pessoal de Nível Superior<br>Skin wounds are interruptions of the normal physiological and anatomical structure of the skin causing damage by loss of barrier function becoming the organism exposed to various types of substances and microorganisms. A fast healing of the wound is essential to avoid the risk of infections and other complications. The aim of this work w
APA, Harvard, Vancouver, ISO, and other styles

Book chapters on the topic "Lipid-core polymeric nanoparticles"

1

Jain, Anamika, Laxmikant Gautam, Nikhar Vishwakarma, et al. "Emergence of Polymer-Lipid Hybrid Systems in Healthcare Scenario." In Multifunctional Nanocarriers for Contemporary Healthcare Applications. IGI Global, 2018. http://dx.doi.org/10.4018/978-1-5225-4781-5.ch017.

Full text
Abstract:
Nanotechnology has drawn the attention of many researchers for the delivery of therapeutics used in various medical applications. Liposomes and polymeric nanoparticles represent promising nanocarriers that efficiently encapsulate drugs, which prevents their degradation along with the control and sustained drug release. Despite the many advantages of these formulations, some of the drawbacks associated with them limit their application to a certain extent. Therefore, there is need for a novel nanocarrier that possesses all of their individual advantages and excludes their drawbacks. Currently, researchers are focused on developing a novel platform that is a hybrid of a polymeric and liposomal-based carrier that combines the peculiarity of both and excludes their shortcomings. Lipid hybrid polymer nanoparticles (LPNs) contain the hydrophobic biodegradable polymeric core surrounded by a lipid layer for intensification of biocompatibility. This chapter includes an introduction of LPNs along with their advantages, composition, and method of preparation.
APA, Harvard, Vancouver, ISO, and other styles
2

Jain, Anamika, Laxmikant Gautam, Nikhar Vishwakarma, et al. "Emergence of Polymer-Lipid Hybrid Systems in Healthcare Scenario." In Research Anthology on Synthesis, Characterization, and Applications of Nanomaterials. IGI Global, 2021. http://dx.doi.org/10.4018/978-1-7998-8591-7.ch006.

Full text
Abstract:
Nanotechnology has drawn the attention of many researchers for the delivery of therapeutics used in various medical applications. Liposomes and polymeric nanoparticles represent promising nanocarriers that efficiently encapsulate drugs, which prevents their degradation along with the control and sustained drug release. Despite the many advantages of these formulations, some of the drawbacks associated with them limit their application to a certain extent. Therefore, there is need for a novel nanocarrier that possesses all of their individual advantages and excludes their drawbacks. Currently, researchers are focused on developing a novel platform that is a hybrid of a polymeric and liposomal-based carrier that combines the peculiarity of both and excludes their shortcomings. Lipid hybrid polymer nanoparticles (LPNs) contain the hydrophobic biodegradable polymeric core surrounded by a lipid layer for intensification of biocompatibility. This chapter includes an introduction of LPNs along with their advantages, composition, and method of preparation.
APA, Harvard, Vancouver, ISO, and other styles
3

"- Folic Acid Conjugated Nanoparticles of Mixed Lipid Monolayer Shell and Biodegradable Polymer Core for Targeted Delivery of Docetaxel." In Chemotherapeutic Engineering. Jenny Stanford Publishing, 2014. http://dx.doi.org/10.1201/b15645-25.

Full text
APA, Harvard, Vancouver, ISO, and other styles
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!