Antiviral agents formulations

FDA approved intraocular injections include mio-tics, viscoelastics, and viscoadherents and an antiviral agent for intravitreal injection. The approved intraocular miotics, carbachol (Miostat ) and acetylcholine (Miochol ), are injected into the anterior chamber at the end of cataract surgery to constrict the pupil and allow the iris to cover the implanted intraocular lens. Carbachol is formulated in a BSS vehicle in sterile water for injection at a physiological pH... 

A new antiviral agent, developed for treatment of CMV retinitis, can be administered by intravitreal injection. Formivirsen sodium is a phosphorothioate oligonucleotide that inhibits CMV replication through an antisense mechanism. It is formulated as a sterile and preservative-free solution and supplied in single-use vials (Vitravene ). The product is administered directly into the vitreous cavity posterior to the limbus through a 30-gauge needle. This procedure can be performed on an... 

In paint formulations of idoxuridine, dimethyl sulfoxide acts both as a solvent to increase drug solubility and a means of enabling penetration of the antiviral agent to the deeper levels of the epidermis. See Table I. 

In its original formulation as a hard gel capsule (saquinavir-H Invirase), oral saquinavir was poorly bioavailable (about 4% in the fed state). It was therefore largely replaced in clinical use by a soft gel capsule formulation (saquinavir-S Fortovase), in which absorption was increased approximately threefold. However, reformulation of saquinavir-H for once-daily dosing in combination with low-dose ritonavir (see Ritonavir) has both improved antiviral efficacy and decreased the gastrointestinal side effects typically associated with saquinavir-S. Moreover, coadministration of saquinavir-H with ritonavir results in blood levels of saquinavir similar to those associated with saquinavir-S, thus capitalizing on the pharmacokinetic interaction of the two agents. 

Phosphorus-containing sugar analogues have possible medicinal application in the treatment of obesity and diabetes, and also in the formulation of antiviral, antibiotic and antitumor agents (Section 6.25.5.2.1.ii) <94JOC2976>. 

Famciclovir, the oral formulation of penciclovir, is a new antiherpes agent that is well absorbed following oral administration with little intersubject variability, and is rapidly converted to penciclovir with a bioavailability of 77%. Furthermore, although the activities of penciclovir and acyclovir against varicella-zoster virus (VZV) in infected cell lines appear to be comparable, penciclovir-triphosphate persists in virus-infected cells far longer than acyclovir-triphosphate, resulting in more prolonged antiviral activity. The intracellular half-life of penciclovir-triphosphate in VZV-infected cells is reported to be 9 hours, whereas that of... 

Silver sulfadiazine (SSD) is one of the most widely used silver compounds in antimicrobial formulations. When introduced iu 1968, SSD was recommended as a topical treatment agent for the prevention of pseudomonad infections in bums. It has since been demonstrated to possess broad-spectrum autibacterial, antifungal, and antiviral activity. 

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