Health Benefits of Garlic .
Garlic contains, sulphur compounds , aged garlic when finely chopped and aged it contains amino acid allicin which is diallyl thiosulphinate , which in turn is beakdown in to diallyl disulphide . Disulphide and thiosulphinate groups, because of their strong reducing properties are capable of even reacting with oxidizing free radicals and peroxides in our body which are responsible for effect of aging, also these moieties can inhibit oxidase enzymes which are responsible harmful oxidative effect on body tissues.
Garlic also contain flavonoids which are antioxidant and are known to protect body against oxidative process of aging.
In some animal experiments it is observed that garlic is able to protect DNA from oxidative damage and mutation, hence many researchers are looking at garlic as a natural protective remedy against cancer, it is believed that regular use of aged garlic can protect our body from certain types of cancers.
Regular use of garlic in food as additional supplement is beneficial in several ways.
Garlic is can lower down aging and oxidative process of body and protect our body from harmful effect of free radicals.
Garlic is known to reduce total cholesterol and LDL in some individuals , but it is not yet firmly established or proved in any clinical trial.
Property of garlic to induce thinning of blood is considered as a cardio protective property which helps to keep away thromoembolic conditions.
Garlic is helpful in arthritis , and has cardioprotective properties .
Garlic supplementation is found to be useful in reducing blood pressure.
Aging process:
Human body is complex system that functions in normal condition due to number of physiological events and biochemical cycles , human body synthesize number of indigenous biomolecules and biochemicals , which take part in completion of several functions which are responsible for normal functioning of our body.
As age progresses these physiological events and systems or biochemical mechanisms become weaker and some times , the biochemicals those were helping our body earlier , may prove bit harmful this time, this is a process of aging.
One of the most important factor in aging is oxidative process , faster oxidation of bimolecules
or proteins , enzymes , which are responsible for some critical physiological functions.
Many peoples take antioxidant food suppliments in order to over come the process of aging , we sugest that one should consult with physician before starting antioxidant food suppliments
Warning:
As that with any drug molecule, garlic has its own side effects , garlic too has its own adverse effects and has many drug interactions which are stll not clearly known.
Hence before starting garlic one should first consult your physician or Doctor.
If you are taking any sort of medication, then do not take garlic concomitantly or do not take garlic even after a break of few days(wash out period) so as to avoid harmful side effects of garlic when combined with other drugs.
Garlic can interfere with number of drugs , a pharmacist and doctors can visualize them , but data is very limited.
One of the important drug interaction reported so far is with anti retroviral drug , garlic can lower the efficacy of antiretroviral drug (competitive inhibition) , hence patients on HAART regimen (that include protease inhibitors ) should not take garlic supplements.
Garlic is known to produce extended coagulation time hence person consuming garlic supplements may be at risk of blood loss in accidental injuries, hence garlic should not be taken while some one is already taking a anticoagulant drugs like warfarin, aspirin etc.
=====================================================================================================
Do you know now this website has become a most popular and most referred website in pharmaceutical industry and pharmaceutical companies and pharmaceutical manufacturers from all over the world ,for almost all topics related to Pharmaceutical Manufacturing , Pharmaceutical Regulatory Affairs and Good Manufacturing Practice for Pharmaceutical Manufacturing (c GMP guidelines ) and latest news and new drugs developments.
=====================================================================================================
You may also like following articles
What is Generic Drug
What is Referance Listed Drug ? ( RLD )
What is Pharmaceutical Equivalents
What is Pharmaceutical Alternatives
What is Therapeutic Equivalents
Why a drug is bound to protein, What is protein binding? What is drug absorption , distribution ?
Do Physical properties contribute to drug activity.
What is drug receptor , How a drug resistance occurs
Mechanism of drug resistance
What is drug interaction
Drug interaction, and its examples
What is first pass metabolism of a drug
What is What is 510(k) Clearances ?
What is 510(k) Clearances,
Premarket Notification for medical devices - PMN or 510(k)
What is a drug interaction
Examples of drug interactions
Antibiotic Definition and classification
Antibiotic resitance and Antibiotic resistance mechanism
Antioxidants food suppliments
Vitamin D Details on FDA cautions on accurate dosage of Vitamin D
What is an antibody? what is monoclonal and polyclonal antibodies?
Terminologies In vaccine Production
Multi stage testing of Virus vaccine production
Testing of vaccines at different stages of production
TESTING FOR ADVENTITIOUS AGENTS CELL PROPERTIES IN VIRAL VACCINE PRODUCTION
Enzyme linked immunosorbent assay ELISA
Raido Immuno assay
http://whoguideline.blogspot.com/2010/04/terminalogy-and-their-explanations.html
Pharmaceutical Aseptic Manufacturing Process Terms , Terminology and Definitions.
http://whoguideline.blogspot.com/2010/02/pharmaceutical-aseptic-manufacturing.html
Here are some articles which will be useful for you in further understanding of aspects of sterile dosage form manufacturing and regulatory affairs and good manufacturing practice in
pharmaceutical industry
Pharmaceutical Validation
Types of validations in pharmaceutical manufacturing
Requirements of documents for validation of sterilisation process
How to investigate OOS out of specification results
Determination of Phenol coefficient of a disinfectant
Sterility testing
Cleen Room Classification
Time limitations in sterile pharmaceuticals processing
Aspects of validation of manufacturing process in sterile pharmaceuticals
Clinical Trials
Controlling Pyrogens in injectable dosage forms
Media fill run process simulation aspects Validation of Aseptic Process and Sterilisation
New Drug Application (NDA) how to make a New Drug Application (NDA) to US FDA
Abbreviated New Drug Application (ANDA) What is ANDA , detaied information about ANDA preparation and submission to US FDA
How to make Investigational New Drug (IND) Application to US FDA
Drug applications submission to us fda Over the counter Drugs OTC drugs
BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS
Electronic record in pharmaceutical manufacturing industry
Good manufacturing practice in pharmaceutical industry
Pharmaceutical industry pharmaceutical companies and FDA latest updates
Here is an interesting article on world wide pharmaceutical industry and making a carrier in one of pharmaceutical companies article on Pharmaceutical Industry pharmaceutical industry
Find a Job in Pharmaceutical Company -->JOBS IN PHARMA INDUSTRY<---
To Find Pharmaceutical jobs and make a Pharmaceutical careers see here pharmaceutical companies
Here are some interesting articles on Quality assurance systems for pharmaceutical company
1.Quality assurance in pharma industry
2.Quality by designe concept for pharmaceutical industry
3.Quality by designe concept in pharmaceutical industryan explanation
This website is written by experts in Pharmaceutical Industry Manufacturing Research and Development and Regulatory Affairs Since 2008 and in 2011 Awarded as one of top 10 websites across world in Pharmaceutical Manufacturing Regulatory
USFDA WHO GMP Guidelines Pharmaceutical Regulations Information about Pharma Quality Managment System Validations Process Validation Cleaning Validation Equipment Qualification Equipment Process Validation Computer System Validation Sterile Product Manufacturing Guidelines Media fill guideline Aseptic Techniques in Sterile dosage form Clean Room Clean Room Classification Guidelines on Area Qualification HVAC AHU HEPA Filter HEPA Filter integrity testing and leak test
Subscribe to:
Post Comments (Atom)
Pharma Guidelines Most Read
-
Clean Room Classification aspects of cleanroom requirements in aseptic Process in manufacturing of sterile dosage form. Classification o...
-
Pharmaceutical validation In pharmaceutical manufacturing industry Pharma Validation regulatory requirements. Validation in Pharma Indus...
-
Clean Room classification Pharmaceutical Manufacturing Area Classification particle count What is a clean room in Pharmaceutical Manufactu...
-
Pharma Companies list of Pharma manufacturing companies world wide list Top pharmaceutical companies around the worlds . Here is the...
-
HEPA filter w hat is a High-Efficiency Particulate Air (HEPA) filter, ULPA filters? How HEPA filters work, its efficacy test and test for ...
-
WHO GMP Training Questions and Answers Section for pharmaceutical manufacturing units :-Quality Management In this post i am giving some qu...
-
In earlier article we have discussed in details about what is therapeutic index and what is meant by narrow therapeutic index drug . Her...
-
Definitions of a drug, Radioactive Drug, Radiopharmaceuticals, Investigational New Drug or Device, Drug product, Drug substance, What is an...
-
Definitions and Descriptions of process. Type A cleaning: In a continuous production runs, when the cleaning is done in between the comple...
-
What is 21 CFR Part 11 Title 21 in the federal regulations are regulations which regulates the Food and Drugs in United States of America...
.
-
Clean Room Classification aspects of cleanroom requirements in aseptic Process in manufacturing of sterile dosage form. Classification o...
-
Pharmaceutical validation In pharmaceutical manufacturing industry Pharma Validation regulatory requirements. Validation in Pharma Indus...
-
Corrective and Preventive Action CAPA What is meant by CAPA In Pharma As the title itself suggest CAPA is an important function of qualit...
-
Clean Room classification Pharmaceutical Manufacturing Area Classification particle count What is a clean room in Pharmaceutical Manufactu...
-
Good Manufacturing Practices guidelines its importance in (gmp guidelines) For Pharmaceutical Industry. A drug , medical device can b...
-
Definitions of a drug, Radioactive Drug, Radiopharmaceuticals, Investigational New Drug or Device, Drug product, Drug substance, What is an...
-
In earlier article we have discussed in details about what is therapeutic index and what is meant by narrow therapeutic index drug . Her...
-
Media Fill Run to ensure the sterility Sterile dosage form evaluation of manufacturing process by Process Simulations /media fill run Val...
-
Lyophilisation Freez Drying : When we think about drying process in pharmaceutical manufacturing process, we think of application of he...
-
Ebola virus infection is life threatening almost 95% of infected people lost their life. Only in few instance in USA hospitals like Nebrask...
Readers Visit Number
This website is Authentic Source of Pharmaceutical Guidelines
Pharma Validations Quality Management System USFDA Guidelines WHO GMP Guidelines New Drug Update
This website consist of detail Information about Pharma Guidelines Pharma Regulatory Affairs USFDA Guidelines WHO Guidelines Pharmaceutical Quality Management System Pharma Validations Process Validation Cleaning Validation Equipment Qualification Equipment Process Validation Computer System Validation Sterile Product Manufacturing Guidelines Media fill guideline Aseptic Techniques in Sterile dosage form Clean Room Clean Room Classification Guidelines on Area Qualification HVAC AHU HEPA Filter HEPA Filter integrity testing and leak test
No comments:
Post a Comment