lördag 30 augusti 2014

Drug-Drug/Drug-Excipient Compatibility Studies on Curcumin using Non-Thermal Methods

Drug-Drug/Drug-Excipient Compatibility Studies on Curcumin using Non-Thermal Methods





Introduction

Curcumin is a hydrophobic polyphenol isolated from dried rhizome of turmeric (Curcuma Longa Linn & zingiberaceae family), which is responsible for various pharmacological activities including anti-cancer, anti-oxidant, anti-bacterial, anti-fungal, anti-viral and anti-inflammatory and expected to have medicinal benefits in arthritis, psoriasis, diabetes, acquired immunodeficiency syndrome, cardiovascular diseases, multiple sclerosis, cancer and lung fibrosis., However, clinical usefulness of curcumin in the treatment of cancer is limited due to poor aqueous solubility, hydrolytic degradation in alkaline pH, metabolism via glucuronidation and sulfation in the liver and in intestine, and poor oral bioavailability. These limitations results in decreased therapeutic efficacy or absence of therapeutic efficacy in in-vivo studies. Though there are many novel approaches to overcome these limitations, nanotechnology (Particle size <1000 nm) is the most recent and offer significant improvement., Hence, to overcome these limitations we proposed to fabricate curcumin-piperine, curcumin-quercetin and curcumin-silibinin loaded polymeric nanoformulation. However, unfavourable combinations of drug-drug and drug-excipient may result in interaction, which leads to physical instability or chemical instability. Physical instability refers to changes in the characteristics of a drug that do not involve chemical bond formation or breakage in the drug structure, which can be identified by changes in the organoleptic parameters such as appearance, form etc. Chemical instability refers to changes in the chemical structure of the drug molecule resulting in drug degradation, reduced drug content and formation of other molecule such as degradation products. Both physical and chemical instability may cause safety concerns. Hence, a thorough drug-drug/drug-excipient compatibility study is mandatory. The present study was aimed to assess the physical and chemical instability of curcumin with various excipients to be used in the proposed nanoformulations.

måndag 21 juli 2014

The Ultimate Hack – Collective Bio Hacking – Who Wants To Join?


De första resultaten av en studie som jag var med i, har precis kommit in o blivit tolkade. Resultaten kan vara intressant för de som är intresserad av Blodsockernivåer och Keton nivåer. Resultaten hittills visar att man kan sänka sitt blodsocker trots att man äter 40 gram kolhydrater vid ett tillfälle! Vi är än så länga bara 2 som har fullföljt studien men fler förväntas göra alla tester.


Studien är utformat på följande vis:

vi tittade på hur Bulletproof kaffe, vassleprotein, kreatin, kokosfett, Brain oktane och maltodextrin påverkar blodglukos och keton nivå. Vi mäter på fastande mage, innan o  1 timma efter intag. Totalt 17 dagar mäter vi med olika kombinationer.


Testet tog form på Bulletproof forum o här är en länk till tråden


Info:


Patrik går igenom resultaten i en video som finns länkad i PDF:en som man kan ladda ner gratis om man anger sin e-postaddress på följande länk.



Jag tycker resultatet är riktigt spännande hoppas ni också finner det intressant