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General
- Aciclovir (INN)or
acyclovir (USAN, former BAN), chemical name acycloguanosine, is a
guanine analogue antiviral drug.
- Aciclovir was seen as
the start of a new era in antiviral therapy.
- Aciclovir differs
from previous nucleoside analogues in that it contains only a partial
nucleoside structure.
- Acyclovir is poorly
water soluble and has poor oral bioavailability.
- Acyclovir is
available with a prescription under the brand name Zovirax.
- Acyclovir is
prescribed as a cream or ointment (topical use), oral tablets, or
intravenous liquid.
Process
- Acyclovir is highly
selective due to its affinity for the enzyme thymidine kinase (TK)
encoded by HSV and VZV. This viral enzyme converts acyclovir into
acyclovir monophosphate, a nucleotide analogue.
- The comparability of
systemic aciclovir exposure at steady state in immunocompromised
patients has been evaluated.
- Two common hydrolytic
enzymes were used as the catalysts for the transesterification of
acyclovir.
- The antiviral action
of acyclovir involves its enzymatic conversion into the triphosphate of
acycloguanosine 9-[(2-hydroxyethoxy)methyl]guanine}.
- Acyclovir
{9-[(2-hydroxyethoxy)methyl]guanine} is a synthetic purine nucleoside
analog derived from guanine.
Application
- Acylovir is indicated
for the treatment of HSV and VZV infections.
- Taking acyclovir with
food may decrease stomach upset.
- Acyclovir is used to
treat infections caused by herpes viruses.
- Acyclovir is a purine
nucleoside analogue with effects against human herpesvirus infections.
- Antiviral nucleoside
acyclovir acts as a potential drug candidate for improving antiviral
efficacy against herpetic epithelial and stromal keratitis.
- The use of acyclovir
(ACV) has become an established part of clinical practice.
Technology
- HPLC technique is
used for the determination of guanine nucleoside derivative acyclovir in
serum, saliva and urine.
- Inderting Acyclovir
twice a day by melt extrusion technique helps to improve patient
complience using hydroxypropylcellulose as thermoplastic polymer.
- Suppression and
reactivation of viral replication were evaluated by functional and
molecular techniques.
- The effect of solvent
polarity on the keto–enol tautomerism of N- and O-acetylated acyclovir
derivatives has been studied through different spectroscopic technique.
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