Pharmacokinetics of thiamine derivatives especially of benfotiamine.

Loew D.

Wuppertal, Germany.
Int J Clin Pharmacol Ther. 1996 Feb;34(2):47-50. 

Abstract

Pharmacokinetic data of orally administered lipid-soluble thiamine analogues like benfotiamine are reviewed and assessed.  It is quite clear that benfotiamine is absorbed much better than water-soluble thiamine salts: maximum plasma levels of thiamine are about 5 times higher after benfotiamine, the bioavailability is at maximum about 3.6 times as high as that of thiamine hydrochloride and better than other lipophilic thiamine derivates. The physiological activity (alphaETK) increased only after benfotiamine was given. Due to its excellent pharmacokinetic profile benfotiamine should be preferred in treatment of relevant indications.

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  1.   Benfotiamine  prevents diabetic side effects
  2.   Benfotiamine  a new approach to preventing diabetic retinopathy
  3.   Benfotiamine  delays formation of advanced glycosylation end-products
  4.   Benfotiamine  effectiveness in diabetic neuropathy 
  5.   Benfotiamine  efficacy in diabetic polyneuropathy 
  6.   Benfotiamine  efficacy in patients diabetic neuropathy
  7.   Benfotiamine  bioavailability 
  8.   Benfotiamine  treatment of diabetic polyneuropathy 
  9.   Benfotiamine  is indicated in end-stage renal disease 
10.   Benfotiamine  may prevent diabetic complications
11.   Benfotiamine  inhibits formation of advanced glycation end products
12.   Benfotiamine  suppressed the formation of advanced glycation end products

 

 

 

 

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