Insoluble Drug Delivery Microparticle

We have collected information about Insoluble Drug Delivery Microparticle for you. Follow the links to find out details on Insoluble Drug Delivery Microparticle.


Microparticles as Controlled Release Drug Delivery Systems

    https://lubrizolcdmo.com/wp-content/uploads/2019/10/AAPS-Presentation-on-Microparticles.pdf
    Microparticle Advantages • Effective delivery of insoluble actives • Bolus delivery instead slower IV administration • Targeted drug delivery to specific sites • Reduction of dose frequency and toxicity • Ability to maintain drug in amorphous form • Reduction of local side effects • Maintenance of therapeutic plasma concentrations 8

An open-label, crossover study of the pharmacokinetics of ...

    https://www.ncbi.nlm.nih.gov/pubmed/16490579
    An open-label, crossover study of the pharmacokinetics of Insoluble Drug Delivery-MicroParticle fenofibrate in combination with atorvastatin, simvastatin, and extended-release niacin in healthy volunteers. Penn R(1), Williams RX 3rd, Guha-Ray DK, Sawyers WG, Braun SL, Rains KT.Author: Ruth Penn, Robert X. Williams, Dilip K. Guha-Ray, William G. Sawyers, Sandra L. Braun, Keith T. Rain...

Complex microparticle architectures from stimuli ...

    https://www.nature.com/articles/s41467-020-15128-9
    Mar 12, 2020 · Because ELPs consist of VPGXG repeats (Fig. 1a) found in tropoelastin, they are non-toxic and biocompatible, leading to their extensive application in drug delivery and tissue engineering …Author: Stefan Roberts, Vincent Miao, Simone Costa, Joseph Simon, Garrett Kelly, Tejank Shah, Stefan Zausche...

Microparticles as controlled drug delivery carrier for the ...

    https://www.sciencedirect.com/science/article/pii/S131901641400111X
    Controlled release drug delivery includes carriers such as polymer-based disks, microparticles, nanoparticles, pellets in which drug gets encapsulated and release at controlled rates for relatively long periods of time. Such kind of systems often show several …Author: Nidhi, Muzamil Rashid, Veerpal Kaur, Supandeep Singh Hallan, Saurabh Sharma, Neeraj Mishra

(PDF) Micro particles: An approach for betterment of drug ...

    https://www.researchgate.net/publication/216063311_Micro_particles_An_approach_for_betterment_of_drug_delivery_system
    throughput screening and in silico three dimensional drug design has yielded drug candidates with low water solubility and thus an inherently low mucosal permeability which makes the development ...

MICROPARTICLE: A NOVEL DRUG DELIVERY SYSTEM

    http://www.ijpbs.com/ijpbsadmin/upload/ijpbs_518f888512e54.pdf
    drug delivery. Another advantage is that particles in the magnetic fluid interact strongly with each other, which facilitates the delivery of high concentrations of drug to targeted areas.5 Magnetic microspheres can be filled with drugs or radioactive materials to treat a …

An open-label, crossover study of the pharmacokinetics of ...

    https://www.researchgate.net/publication/7285811_An_open-label_crossover_study_of_the_pharmacokinetics_of_Insoluble_Drug_DeliveryR-MicroParticle_fenofibrate_in_combination_with_atorvastatin_simvastatin_and_extended-release_niacin_in_healthy_voluntee
    Insoluble Drug Delivery-Microparticle (IDD-P) fenofibrate 160-mg tablets are a new formulation developed to provide bioavailability independent of food.

Bioerodable PLGA-Based Microparticles for Producing ...

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4923250/
    Jun 28, 2016 · Any water insoluble material can be used as the microparticle matrix to produce the desired drug release profiles, and microparticles are recovered from the readily soluble hydrogel templates. The technology allows for precise control of the size and shape of template wells in every dimension so that microparticles with a narrow size distribution can be produced (Lu et al., 2014 ; …Author: Felicity Y. Han, Kristofer J. Thurecht, Andrew K. Whittaker, Maree T. Smith

An open-label, crossover study of the pharmacokinetics of ...

    https://www.sciencedirect.com/science/article/abs/pii/S0149291805003164
    An open-label, crossover study of the pharmacokinetics of Insoluble Drug Delivery®-MicroParticle fenofibrate in combination with atorvastatin, simvastatin, …Author: Ruth Penn, Robert X. Williams, Dilip K. Guha-Ray, William G. Sawyers, Sandra L. Braun, Keith T. Rain...

Searching for Insoluble Drug Delivery Microparticle?

You can just click the links above. The data is collected for you.

Related Delivery Info