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Drug Delivery Application

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https://www.readbyqxmd.com/read/30110614/the-molecularly-imprinted-polymer-essentials-curation-of-anticancer-ophthalmic-and-projected-gene-therapy-drug-delivery-systems
#1
REVIEW
Christian Antonio Tuwahatu, Chi Chung Yeung, Yun Wah Lam, Vellaisamy Arul Lenus Roy
The development of polymeric materials as drug delivery systems has advanced from systems that rely on classical passive targeting to carriers that can sustain the precisely controlled release of payloads upon physicochemical triggers in desired microenvironment. Molecularly imprinted polymers (MIP), materials designed to capture specific molecules based on their molecular shape and charge distribution, are attractive candidates for fulfilling these purposes. In particular, drug-imprinted polymers coupled with active targeting mechanisms have been explored as potential drug delivery systems...
August 12, 2018: Journal of Controlled Release: Official Journal of the Controlled Release Society
https://www.readbyqxmd.com/read/30110473/synthesis-of-1-8-naphthalimide-based-probes-with-fluorescent-switch-triggered-by-flufenamic-acid
#2
G Saito, D Velluto, M Resmini
In this work, we report the synthesis of novel fluorescent molecules, based on 1,8-naphthalimide thio- and amino-derivatives, designed to display an OFF-ON and ON-OFF photoelectron transfer fluorescence switch upon interaction with a proton-donor drug. We have functionalized the new probes to allow easy formation of a covalent link to polymer matrices, for future applications as drug delivery sensors. We have investigated the fluorescent switch of the new probes using flufenamic acid (FA, pKa 3.65), a water insoluble, non-steroidal anti-inflammatory drug, as a model drug and proton source...
June 2018: Royal Society Open Science
https://www.readbyqxmd.com/read/30110449/functional-materials-based-on-molecules-with-hydrogen-bonding-ability-applications-to-drug-co-crystals-and-polymer-complexes
#3
REVIEW
Kristin M Hutchins
The design, synthesis and property characterization of new functional materials has garnered interest in a variety of fields. Materials that are capable of recognizing and binding with small molecules have applications in sensing, sequestration, delivery and property modification. Specifically, recognition of pharmaceutical compounds is of interest in each of the aforementioned application areas. Numerous pharmaceutical compounds comprise functional groups that are capable of engaging in hydrogen-bonding interactions; thus, materials that are able to act as hydrogen-bond receptors are of significant interest for these applications...
June 2018: Royal Society Open Science
https://www.readbyqxmd.com/read/30110129/conjugated-polymer-nanoparticles-appending-photo-responsive-units-for-controlled-drug-delivery-release-and-imaging
#4
Shu Wang
Carriers that can afford tunable physical and structural changes are envisioned to address critical issues in controlled drug delivery applications. Herein, we report photo-responsive conjugated polymer nanoparticles (CPNs) functionalized with donor-acceptor Stenhouse adduct (DASA) and folic acid units for controlled drug delivery, release and imaging. Upon visible light (λ = 550 nm) irradiation, CPNs undergo structure, color, and polarity changes simultaneously that swell and open-up CPNs to release encapsulated drugs into the medium and cells...
August 15, 2018: Angewandte Chemie
https://www.readbyqxmd.com/read/30109926/on-demand-degradation-of-metal-organic-framework-based-on-photocleavable-dianthracene-based-ligand
#5
Guillaume Collet, Timothée Lathion, Céline Besnard, Claude Piguet, Stéphane Petoud
We have designed a rigid photocleavable dianthracene-based ligand that reacts with ytterbium as coordination metal ion for the creation of a class of tridimensional light-degradable metal-organic framework (MOF). We demonstrated that we can obtain a high level of control on the disassembly of the MOF formed with this ligand which can be triggered either through light irradiation or temperature increase. The reversible 4π-4π photodimerization is the intrinsic chemical mechanism ruling the ligand and MOF cleavage...
August 15, 2018: Journal of the American Chemical Society
https://www.readbyqxmd.com/read/30109346/synthesis-of-next-generation-dual-responsive-cross-linked-nanoparticles-and-their-application-to-anti-cancer-drug-delivery
#6
Christina Schwarzenböck, Peter J Nelson, Ralf Huss, Bernhard Rieger
Rare earth metal-mediated group transfer polymerisation enables the synthesis of previously inaccessible block copolymers of 2-vinylpyridine, diethyl vinylphosphonate and the new diallyl vinylphosphonate monomer. This precision polymerisation and the selective cross-linking of allyl side groups via thiol-ene click chemistry leads to the formation of well-defined dual-responsive nanoparticles. We demonstrate that these next generation nanocarriers are pH- and temperature-responsive and are capable of efficiently delivering doxorubicin into the nucleus of cancer cells...
August 15, 2018: Nanoscale
https://www.readbyqxmd.com/read/30109320/a-supramolecular-hybrid-material-constructed-from-pillar-6-arene-based-host-guest-complexation-and-zif-8-for-targeted-drug-delivery
#7
Kui Yang, Ke Yang, Shuang Chao, Jia Wen, Yuxin Pei, Zhichao Pei
A novel supramolecular hybrid material ZIF-8@DOX@WP6@G constructed from the host-guest complexation between carboxylated pillar[6]arene (WP6) and a galactose derivative (G), and doxorubicin (DOX)-loaded ZIF-8 has been synthesized for targeted drug delivery. The results showed that ZIF-8@DOX@WP6@G not only maintained the pH-sensitive drug release properties of ZIF-8 but also exhibited excellent water dispersibility and selective toxicity for hepatoma cancer cells due to the assembly of WP6 and G. The strategy used in this study opens up a new avenue for constructing multifunctional supramolecular hybrid materials for therapeutic applications in cancer treatment...
August 15, 2018: Chemical Communications: Chem Comm
https://www.readbyqxmd.com/read/30109147/a-review-on-the-use-of-magnetic-fields-and-ultrasound-for-non-invasive-cancer-treatment
#8
REVIEW
Somoshree Sengupta, Vamsi K Balla
Current popular cancer treatment options, include tumor surgery, chemotherapy, and hormonal treatment. These treatments are often associated with some inherent limitations. For instances, tumor surgery is not effective in mitigating metastases; the anticancer drugs used for chemotherapy can quickly spread throughout the body and is ineffective in killing metastatic cancer cells. Therefore, several drug delivery systems (DDS) have been developed to target tumor cells, and release active biomolecule at specific site to eliminate the side effects of anticancer drugs...
November 2018: Journal of Advanced Research
https://www.readbyqxmd.com/read/30109086/primary-biocompatibility-tests-of-poly-lactide-co-glycolide-poly-l-orithine-fucoidan-core-shell-nanocarriers
#9
Duanhua Cai, Jingqian Fan, Shibin Wang, Ruimin Long, Xia Zhou, Yuangang Liu
Layer-by-layer (LbL) self-assembly is the technology used in intermolecular static electricity, hydrogen bonds, covalent bonds and other polymer interactions during film assembling. This technology has been widely studied in the drug carrier field. Given their use in drug delivery systems, the biocompatibility of these potential compounds should be addressed. In this work, the primary biocompatibility of poly(lactide-co-glycolide)-(poly-L-orithine/fucoidan) [PLGA-(PLO/fucoidan)] core-shell nanoparticles (NPs) was investigated...
July 2018: Royal Society Open Science
https://www.readbyqxmd.com/read/30108889/synthesis-of-surface-capped-mesoporous-silica-nanoparticles-for-ph-stimuli-responsive-drug-delivery-applications
#10
Madhappan Santha Moorthy, Subramanian Bharathiraja, Panchanathan Manivasagan, Kang Dae Lee, Junghwan Oh
Mesoporous silica-based drug delivery carriers mostly require appropriate surface modifications to improve their drug delivery efficiency and to reduce their adverse side effects. In the present work, we have synthesised mesoporous silica nanoparticles and their surface was covered by using capping units such as tetrathio-maleimide (TTM) via a "host-guest" complexation mechanism for pH-responsive drug delivery applications. The surface-functionalised melamine (Mela) groups on the outer surface of the mesoporous silica nanoparticles act as "hosts" and the surface capped TTM units act as "guests" during the surface capping of the mesoporous silica nanoparticles via the "host-guest" complexation approach...
September 1, 2017: MedChemComm
https://www.readbyqxmd.com/read/30108887/polyhydroxyalkanoates-as-biomaterials
#11
REVIEW
Bhagyashri S Thorat Gadgil, Naresh Killi, Gundloori V N Rathna
Polyhydroxyalkanoates (PHAs) are biopolymers synthesized by bacteria under unbalanced growth conditions. These biopolymers are considered as potential biomaterials for future applications because they are biocompatible, biodegradable, and easy to produce and functionalize with strong mechanical strength. Currently, PHAs are being extensively innovated for biomedical applications due to their prerequisite properties. The wide range of biomedical applications includes drug delivery systems, implants, tissue engineering, scaffolds, artificial organ constructs, etc...
September 1, 2017: MedChemComm
https://www.readbyqxmd.com/read/30107727/fabrication-of-acidic-ph-cleavable-polymer-for-anti-cancer-drug-delivery-using-a-dual-functional-monomer
#12
Luping Zheng, Xiaolong Zhang, Yunfei Wang, Fangjun Liu, Jinlei Peng, Xuezhi Zhao, Huiru Yang, Liwei Ma, Baoyang Wang, Cong Chang, Hua Wei
The preparation of tumor acidic pH-cleavable polymers generally requires tedious post-polymerization modifications, leading to batch-to-batch variation and scale-up complexity. To develop a facile and universal strategy, we reported in this study design and successful synthesis of a dual functional monomer, a-OEGMA that bridges a methacrylate structure and oligo(ethylene glycol) (OEG) units via an acidic pH-cleavable acetal link. Therefore a-OEGMA integrates (i) the merits of commercially available oligo(ethylene glycol) monomethyl ether methacrylate (OEGMA) monomer, i...
August 14, 2018: Biomacromolecules
https://www.readbyqxmd.com/read/30107341/3-hydroxycoumarin-loaded-vesicles-for-recombinant-human-tyrosinase-inhibition-in-topical-applications
#13
Michele Schlich, Marco Fornasier, Mariella Nieddu, Chiara Sinico, Sergio Murgia, Antonio Rescigno
Tyrosinase is one of the key enzymes in mammalian melanin biosynthesis. Decreasing tyrosinase activity has been targeted for the prevention of conditions related to the hyperpigmentation of the skin, such as melasma and age spots. This paper is devoted to the engineering of vesicle formulations loaded with 3-hydroxycoumarin for topical pharmaceutical applications. At first, it was demonstrated the strong inhibiting ability of 3-hydroxycoumarin against recombinant human tyrosinase. Then, such a drug was effectively encapsulated within liquid or gel-like vesicle formulations, both based on monoolein and lauroylcholine chloride...
August 8, 2018: Colloids and Surfaces. B, Biointerfaces
https://www.readbyqxmd.com/read/30106410/nanoscale-mechanics-of-microgel-particles
#14
Anders Aufderhorst-Roberts, Daniel Baker, Richard J Foster, Olivier Cayre, Johan Mattsson, Simon D Connell
Microgel particles are highly tuneable materials that are useful for a wide range of industrial applications, such as drug delivery, sensing, nanoactuation, emulsion stabilisation and use as cell substrates. Microgels have also been used as model systems investigating physical phenomena such as crystallization, glass-formation, jamming, ageing and complex flow behaviour. The responsiveness of microgel systems such as poly(N-isopropylacrylamide) (PNIPAm) to external stimuli has been established in fundamental investigations and in applications and recent work has begun to quantify the mechanics of individual particles...
August 14, 2018: Nanoscale
https://www.readbyqxmd.com/read/30105918/sodium-stibogluconate-loaded-nano-deformable-liposomes-for-topical-treatment-of-leishmaniasis-macrophage-as-a-target-cell
#15
M Junaid Dar, Fakhar Ud Din, Gul Majid Khan
Topical drug delivery against cutaneous leishmaniasis (CL) signifies an effective alternate for improving the availability and reducing the toxicity associated with the parenteral administration of conventional sodium stibogluconate (SSG) injection. The basic aim of the study was to develop nano-deformable liposomes (NDLs) for the dermal delivery of SSG against CL. NDLs were formulated by a modified thin film hydration method and optimized via Box-Behnken statistical design. The physicochemical properties of SSG-NDLs were established in terms of vesicle size (195...
November 2018: Drug Delivery
https://www.readbyqxmd.com/read/30105055/emulsion-cross-linking-technique-for-human-fibroblast-encapsulation
#16
Watcharaphong Chaemsawang, Weerapong Prasongchean, Konstantinos I Papadopoulos, Suchada Sukrong, W John Kao, Phanphen Wattanaarsakit
Microencapsulation with biodegradable polymers has potential application in drug and cell delivery systems and is currently used in probiotic delivery. In the present study, microcapsules of human fibroblast cells (CRL2522) were prepared by emulsion cross-linking technique. Tween 80 surfactant at a 2% concentration through phase inversion resulted in the most efficient and stable size, morphology, and the cells survival at least 50% on day 14. Emulsion cross-linking microcapsule preparation resulted in smaller and possibly more diverse particles that can be developed clinically to deliver encapsulated mammalian cells for future disease treatments...
2018: International Journal of Biomaterials
https://www.readbyqxmd.com/read/30104875/iridium-iii-complex-loaded-liposomes-as-a-drug-delivery-system-for-lung-cancer-through-mitochondrial-dysfunction
#17
Cancheng Liao, Danqiao Xu, Xiaohong Liu, Yuqi Fang, Jun Yi, Xiaofang Li, Bohong Guo
Background and aim: Iridium (Ir)-based complex is a potential antitumor ingredient, but its poor physicochemical properties such as hydrophobicity and low biocompatibility hamper further application. Liposome provides a potential delivery approach for improving the poor physicochemical property and reducing the side effects of antitumor drug. In this study, we aimed at incorporating Ir ([Ir(ppy)2 (BTCP)]PF6 ) into liposomes to enhance the biocompatibility and sustained release of Ir for intravenous administration and to elucidate the mechanism in A549 cells...
2018: International Journal of Nanomedicine
https://www.readbyqxmd.com/read/30104542/sol-gel-silica-nanoparticles-in-medicine-a-natural-choice-design-synthesis-and-products
#18
REVIEW
M Clara Gonçalves
Silica is one of the most abundant minerals in the Earth's crust, and over time it has been introduced first into human life and later into engineering. Silica is present in the food chain and in the human body. As a biomaterial, silica is widely used in dentistry, orthopedics, and dermatology. Recently amorphous sol-gel SiO₂ nanoparticles (NPs) have appeared as nanocarriers in a wide range of medical applications, namely in drug/gene target delivery and imaging diagnosis , where they stand out for their high biocompatibility, hydrophilicity, enormous flexibility for surface modification with a high payload capacity, and prolonged blood circulation time...
August 13, 2018: Molecules: a Journal of Synthetic Chemistry and Natural Product Chemistry
https://www.readbyqxmd.com/read/30104488/lysine-dendrigraft-nanocontainers-influence-of-topology-on-their-size-and-internal-structure
#19
Boris Okrugin, Maxim Ilyash, Denis Markelov, Igor Neelov
Poly-l-ysine dendrigrafts are promising systems for biomedical applications due to their biodegradability, biocompatibility, and similarity to dendrimers. There are many papers about the use of dendrigrafts as nanocontainers for drug delivery. At the same time, the number of studies about their physical properties is limited, and computer simulations of dendrigrafts are almost absent. This paper presents the results of a systematic molecular dynamics simulation study of third-generation lysine dendrigrafts with different topologies...
August 13, 2018: Pharmaceutics
https://www.readbyqxmd.com/read/30103866/matrix-systems-for-oral-drug-delivery-formulations-and-drug-release
#20
REVIEW
Gábor Vasvári, József Kalmár, Péter Veres, Miklós Vecsernyés, Ildikó Bácskay, Pálma Fehér, Zoltán Ujhelyi, Ádám Haimhoffer, Ágnes Rusznyák, Ferenc Fenyvesi, Judit Váradi
In this current article matrix formulations for oral drug delivery are reviewed. Conventional dosage forms and novel applications such as 3D printed matrices and aerogel matrices are discussed. Beside characterization, excipients and matrix forming agents are also enlisted and classified. The incorporated drug could exist in crystalline or in amorphous forms, which makes drug dissolution easily tunable. Main drug release mechanisms are detailed and reviewed to support rational design in pharmaceutical technology and manufacturing considering the fact that R&D members of the industry are forced to obtain knowledge about excipients and methods pros and cons...
July 2018: Drug Discovery Today. Technologies
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