Antiviral Drug Development Service
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Antiviral Drug Development Service

Antiviral drugs are essential medications that seek to control viral infections by preventing replication or other viral activity. At Protheragen, we provide full-service antiviral drug development for unique and specialized ophthalmic diseases.

Overview of Ophthalmic Antiviral Drugs

Viral infections can result in ophthalmic diseases that are complex in nature. If these diseases go untreated, they can progress to severe complications such as vision loss. Antiviral medications are critical in the management of these infections as they work on certain aspects of the viral infection and decrease the burden of the virus on ocular tissues. Herpes simplex keratitis, adenoviral conjunctivitis, and cytomegalovirus retinitis are some of the more common ophthalmic infections that are treated with antivirals. Effective antiviral agents for these diseases include idoxuridine, trifluridine, vidarabine, acyclovir, and ganciclovir. Each has its own mechanism of action and therapeutic index which makes the agents special.

Common inhibitory effects of antiviral drugs. Fig.1 Common inhibitory actions of antiviral drugs. (Kausar S., et al., 2021)

Antiviral Drug Development for Ophthalmic Diseases

Emerging viral pathogens and newer, drug-resistant strains require dynamic and evolving antiviral treatment, which has recently evolved in use and efficacy. New compounds with improved efficacy along with reduced toxicity have been developed in recent advancements in antiviral chemotherapy, suggesting new discoveries adjacent to its use. This includes its oral bioavailability, valacyclovir, which is a prodrug of acyclovir, further highlighting the ongoing research and development importance in improving antiviral therapies alongside its already established safety profile.

Table 1. Approved antiviral agents for viral ophthalmic infections. (Petrillo F., et al., 2022)

Antiviral Chemical Structure Mechanism of Action Target Viruses
Acyclovir Acyclic pyrimidine nucleoside Inhibits viral DNA polymerase; viral DNA chain termination HSV-1, HSV-2, EBV, VZV, CMV
Trifluridine Pyrimidine nucleoside Inhibits thymidylate synthetase Vaccinia virus, HSV-1, HSV-2
Vidarabine Purine nucleoside Inhibits multiple enzymes (e.g., DNA polymerase) CMV, HSV-1, HSV-2 VZV, vaccinia virus, pseudorabies virus
Valaciclovir 1-Valine ester of acyclovir Inhibits viral DNA polymerase; viral DNA chain termination HHV-6, HHV-8, HSV- 1, HSV-2, EBV, VZV, CMV
Valganciclovirn Monovalent ester of ganciclovir Inhibits viral DNA polymerase; viral DNA chain termination VZV, CMV, HSV-1, HSV-2, EBV
Famciclovir Acyclic guanine derivative Inhibits viral DNA polymerase; viral DNA chain termination VZV, HSV- 1, HSV-2, EBV
Idoxuridine Pyrimidine nucleoside Inhibits viral DNA thymidine uptakes, viral DNA polymerases, and viral DNA incorporation HSV-1, HSV-2
Ganciclovir Acyclic pyrimidine nucleoside Inhibits viral DNA polymerase; viral DNA chain termination VZV, CMV, HSV-1, HSV-2, EBV
Cidofovir Phosphonoformic acid derivative Inhibits viral DNA polymerases VZV, CMV, HSV-1, HSV-2 adenovirus, vaccinia virus, EBV
Fomivirsen Antisense oligonucleotide Viral mRNA binding CMV
Foscarnet Phosphonoacetic acid derivative Inhibits viral DNA polymerases and RNA polymerases VZV, CMV, HSV-1, HSV-2, EBV

Disclaimer: Protheragen focuses on providing preclinical research service. This table is for information exchange purposes only. This table is not a treatment plan recommendation. For guidance on treatment options, please visit a regular hospital.

Our Services

Protheragen provides a full-service approach to the unique difficulties posed by ophthalmic diseases within the scope of antiviral drug development. We specialize in all stages of the preclinical development continuum, ranging from the discovery phase to preclinical evaluation.

Target Identification and Validation

The first step involves identifying viral proteins or enzymes that are essential for the virus's replication cycle. These targets are validated through biochemical and genetic approaches to ensure their relevance to the disease.

Types of Antiviral Drugs

  • Nucleoside Analog
  • Non-Nucleoside Inhibitors
  • Glycoprotein Inhibitors
  • DNA Polymerase Inhibitors
  • Broad-Spectrum Antivirals
  • Gene Therapy

Preclinical Testing

This phase includes in vitro and in vivo studies to assess the antiviral activity, pharmacokinetics, and toxicity of the lead compounds. Animal models of ocular infections are used to evaluate the efficacy and safety of the drug candidates.

Formulation Development

We specialize in developing formulations that enhance the delivery and efficacy of antiviral drugs for ophthalmic diseases. Our formulation development services include topical formulations, sustained-release formulations and intravitreal injections.

Solutions for Ophthalmic Diseases

  • Herpes Simplex Keratitis (HSK)
  • Herpes Zoster Ophthalmicus
  • Cytomegalovirus (CMV) Retinitis
  • Adenoviral Conjunctivitis
  • Epstein-Barr Virus (EBV) Keratitis
  • Vaccinia Virus Keratitis
  • Varicella-Zoster Virus (VZV) Iritis
  • Herpes Simplex Virus (HSV) Iritis
  • HSV-Associated Uveitis
  • VZV-Associated Uveitis
  • CMV-Associated Uveitis
  • HSV-Induced Corneal Endothelitis

With our expertise in virology, pharmacology, and ocular biology, Protheragen is your trusted partner in the fight against ocular viral infections. If you are interested in our services, please feel free to contact us.

References

  • Kausar, Shamaila, et al. "A review: Mechanism of action of antiviral drugs." International journal of immunopathology and pharmacology 35 (2021): 20587384211002621.
  • Petrillo, Francesco, et al. "Viral infection and antiviral treatments in ocular pathologies." Microorganisms 10.11 (2022): 2224.