ALUVIA 100/25 TABLETS

Indications

• HIV infection
• AIDS (Acquired Immunodeficiency Syndrome)
• HIV-related opportunistic infections

Dosage

Adults: The recommended dose of lopinavir when used in combination with ritonavir is 400 mg/100 mg taken twice daily or 800 mg/200 mg taken

Mechanism of action

Lopinavir acts as an inhibitor of the HIV-1 protease enzyme, a dimeric aspartic protease that cleaves the Gag polyprotein into functional viral proteins. By mimicking the normal peptide linkage cleaved by the HIV protease, lopinavir prevents the proteolytic cleavage of the Gag polyprotein, leading to the production of immature, non-infectious viral particles. This mechanism disrupts the HIV lifecycle and reduces the infectivity of the virus.

Pharmacodynamics

Lopinavir inhibits the activity of HIV protease, which is critical for HIV maturation. It has a moderate duration of action, necessitating administration once or twice daily. As a protease inhibitor, lopinavir is prone to drug interactions due to its effects on the cytochrome P450 enzyme system. Caution is advised when administering it alongside other medications. Adverse effects may include hepatotoxicity and pancreatitis, particularly in patients with pre-existing risk factors.

Pharmacokinetics

Lopinavir is well absorbed after oral administration, with a bioavailability that can be affected by food. It is metabolized primarily by the liver through the cytochrome P450 system, particularly CYP3A4, which can lead to significant drug interactions. The elimination half-life of lopinavir is approximately 5 to 6 hours, but it can be prolonged when taken with ritonavir. The drug is primarily excreted in the feces, with a small percentage eliminated in the urine.

Contra-indications

• Severe hypersensitivity to lopinavir or any component of the formulation
• Severe hepatic impairment
• Concomitant use with certain drugs that are highly dependent on CYP3A for clearance and that may cause significant drug interactions

Adverse effects

• Nausea
• Diarrhea
• Vomiting
• Abdominal pain
• Headache
• Fatigue
• Hyperlipidemia
• Hepatotoxicity
• Pancreatitis

Interactions

• CYP3A4 inhibitors and inducers
• Anticoagulants
• Anticonvulsants
• Antituberculosis medications
• Hormonal contraceptives

Precautions

• Monitor liver function tests due to risk of hepatotoxicity
• Monitor for signs and symptoms of pancreatitis
• Use with caution in patients with a history of liver disease or pancreatitis
• Evaluate for potential drug-drug interactions before initiating therapy

Pregnancy

Lopinavir is classified as category C. It should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.

Breast-feeding

Lopinavir is excreted in human milk. The decision to continue or discontinue breastfeeding should consider the importance of the drug to the mother.

Storage

Store at room temperature, away from moisture and heat. Protect from light.

Formulations

• Lopinavir/ritonavir combination tablets
• Lopinavir/ritonavir oral solution

Indications

• HIV infection in combination with other antiretroviral drugs

Dosage

Children: For children over 2 years of age

Adults: The typical adult dose of ritonavir is 100–200 mg taken 1–2 times a day. For high-dose ritonavir used as a booster, the recommended dose is 800/200 mg once daily, but this should only be used in patients with an HIV strain that has fewer than 3 mutations to protease inhibitors.

Mechanism of action

Ritonavir inhibits the HIV protease enzyme, which is crucial for the cleavage of the viral polyprotein precursors into functional proteins essential for the formation of infectious HIV particles. By binding to the active site of the protease, ritonavir prevents this cleavage, leading to the production of non-infectious viral particles. Additionally, ritonavir is a potent inhibitor of the cytochrome P450 CYP3A4 isoenzyme, which enhances the pharmacokinetic profile of other protease inhibitors by reducing their metabolism.

Pharmacodynamics

Ritonavir exhibits antiviral activity specifically against HIV-1 by preventing the function of the viral protease. This inhibition disrupts the normal life cycle of HIV, resulting in immature viral particles that cannot propagate infection. Ritonavir is generally administered in conjunction with other antiretroviral therapies to achieve a synergistic effect, enhancing the overall antiviral activity and therapeutic success.

Pharmacokinetics

Ritonavir is well-absorbed when taken orally, with peak plasma concentrations occurring approximately 2 to 4 hours post-administration. Its bioavailability is influenced by food intake. The drug is extensively metabolized in the liver, primarily by the CYP3A4 enzyme. Ritonavir has a half-life of about 3 to 5 hours in adults, requiring multiple daily doses to maintain effective plasma levels. The drug is excreted mainly in feces, with minimal renal excretion.

Contra-indications

• Severe hepatic impairment
• Severe renal impairment
• History of pancreatitis

Adverse effects

• Nausea
• Diarrhea
• Vomiting
• Abdominal pain
• Increased risk of infections
• Pancreatitis
• Hyperlipidemia
• Fat redistribution
• Liver enzyme elevation
• Cardiac conduction disorders
• Visual impairment
• Peripheral neuropathy
• Hypersensitivity reactions

Interactions

• Ritonavir + antipsychotics (second-generation): Severe (affects exposure)
• Ritonavir + clozapine: Severe (affects exposure)
• Ritonavir + benzodiazepines: Severe (increases exposure)
• Ritonavir + diazepam: Severe (increases exposure)
• Ritonavir + flurazepam: Severe (increases exposure)
• Ritonavir + clopidogrel: Severe (decreases efficacy)
• Ritonavir + glecaprevir: Severe (increases exposure)
• Ritonavir + opioids: Severe (increases risk of central nervous system toxicity)
• Ritonavir + pethidine: Severe (increases risk of central nervous system toxicity)
• Ritonavir + tepotinib: Severe (increases exposure)

Precautions

• Monitor liver function tests regularly
• Use with caution in patients with a history of cardiac conduction disorders
• Evaluate signs of pancreatitis, discontinue if diagnosed
• Avoid use in severe impairment of hepatic or renal function
• Consider potential for drug interactions due to CYP3A4 inhibition

Pregnancy

Use during pregnancy only if the potential benefit justifies the potential risk to the fetus. Ritonavir is classified as Category B.

Breast-feeding

Ritonavir is excreted in breast milk. Weigh the benefits of breastfeeding against the potential risks of HIV transmission or adverse effects to the infant.

Storage

Store at room temperature, away from moisture and heat. Keep out of reach of children.

Formulations

• Ritonavir 50 mg tablets

Mechanism of action

The HIV lifecycle is comprised of 3 distinct stages: assembly, involving creation and packaging of essential viral components; budding, wherein the viral particle crosses the host cell plasma membrane and forms a lipid envelope; and maturation, wherein the viral particle alters its structure and becomes infectious. At the center of this lifecycle is the Gag polyprotein which, along with the products of its proteolysis, coordinate these stages and function as the major structural proteins of the virus. The HIV-1 protease enzyme, a dimeric aspartic protease, is the enzyme responsible for cleaving the Gag polyprotein and thus plays a critical role in many aspects of the HIV viral lifecycle. Lopinavir is an inhibitor of the HIV-1 protease enzyme. Its design is based on the "peptidomimetic" principle, wherein the molecule contains a hydroxyethylene scaffold which mimics the normal peptide linkage (cleaved by HIV protease) but which itself cannot be cleaved. By preventing HIV-1 protease activity, and thus the proteolysis of the Gag polyprotein, lopinavir results in the production of immature, non-infectious viral particles. /The researchers/ have previously shown that the HIV protease inhibitor lopinavir has selective toxicity against human papillomavirus (HPV)-positive cervical carcinoma cells via an unknown mechanism. SiHa cervical carcinoma cells were stably transfected with the proteasome sensor vector pZsProSensor-1 to confirm lopinavir inhibits the proteasome in these cells. The Panorama Xpress profiler 725 antibody array was then used to analyse specific changes in protein expression in lopinavir-treated versus control untreated SiHa cells followed by PCR and western blotting. Colorimetric growth assays of lopinavir-treated E6/E7 immortalised versus control human keratinocytes were performed. Targeted small interfering RNA gene silencing followed by growth assay comparison of lopinavir-treated/untreated SiHa cells was also used. Lopinavir induced an increase in the fluorescence of pZsProSensor-1 transfected SiHa cells, indicative of proteasomal inhibition. Ribonuclease L (RNASEL) protein was shown to be up-regulated in lopinavir-treated SiHa cells, which was confirmed by PCR and western blot. Targeted silencing of RNASEL reduced the sensitivity of SiHa cells to lopinavir. Selective toxicity against E6/E7 immortalised keratinocytes versus control cells was also seen with lopinavir and was associated with up-regulated RNASEL expression. These data are consistent with the toxicity of lopinavir against HPV-positive cervical carcinoma cells being related to its ability to block viral proteasome activation and induce an up-regulation of the antiviral protein RNASEL. This is supported by the drug's selective toxicity and up-regulation of RNASEL in E6/E7 immortalised keratinocytes combined with the increased resistance to lopinavir observed in SiHa cells following silencing of RNASEL gene expression. Lopinavir inhibits replication of HIV type 1 (HIV-1) by interfering with HIV protease. During HIV replication, HIV protease cleaves viral polypeptide products of the gag and gag-pol genes to form structural proteins of the virion core and essential viral enzymes. By interfering with the formation of these essential proteins and enzymes, lopinavir blocks maturation of the virus and causes formation of nonfunctional, immature, noninfectious virions. Lopinavir also has some in vitro activity against HIV type 2 (HIV-2).

Pharmacodynamics

Lopinavir inhibits the activity of an enzyme critical for the HIV viral lifecycle. It has a moderate duration of action necessitating once or twice daily dosing. Lopinavir, like other protease inhibitors, has a propensity for participating in drug interactions - use caution when administering lopinavir to patients maintained on other pharmaceutical agents as pharmacodynamic and pharmacokinetic interactions are common. Fatal hepatotoxicity and pancreatitis have been noted in patients undergoing therapy with lopinavir and patients with an increased baseline risk of these events should be monitored closely throughout therapy.

Mechanism of action

Ritonavic inhibits the HIV viral proteinase enzyme that normally cleaves the structural and replicative proteins that arise from major HIV genes, such as *gag* and *pol*. *Gag* encodes proteins involved in the core and the nucleocapsid, while *pol* encodes the the HIV reverse transcriptase, ribonuclease H, integrase, and protease. The *pol*-encoded proteins are initially translated in the form of a larger precursoe polypeptide, *gag-pol*, and needs to be cleaved by HIV protease to form other complement proteins. Ritonavir prevents the cleavage of the *gag-pol* polyprotein, which results in noninfectious, immature viral particles. Ritonavir is a potent inhibitor of cytochrome P450 CYP3A4 isoenzyme present both in the intestinal tract and liver. It is a type II ligand that perfectly fits into the CYP3A4 active site cavity and irreversibly binds to the heme iron via the thiazole nitrogen, which decreases the redox potential of the protein and precludes its reduction with the redox partner, cytochrome P450 reductase. Ritonavir may also play a role in limiting cellular transport and efflux of other protease inhibitors via the P-glycoprotein and MRP efflux channels. Unlike nucleoside antiretroviral agents, the antiviral activity of ritonavir does not depend on intracellular conversion to an active metabolite. Ritonavir and other HIV protease inhibitors (e.g., amprenavir, indinavir, lopinavir, nelfinavir, saquinavir) act at a different stage of the HIV replication cycle than nucleoside and nonnucleoside reverse transcriptase inhibitors, and results of in vitro studies indicate that the antiretroviral effects of HIV protease inhibitors and some nucleoside or nonnucleoside antiretroviral agents may be additive or synergistic. Ritonavir is a selective, competitive, reversible inhibitor of HIV protease. HIV protease, an aspartic endopeptidase that functions as a homodimer, plays an essential role in the HIV replication cycle and the formation of infectious virus. During HIV replication, HIV protease cleaves viral polypeptide products of the gag and gag-pol genes (i.e., p55 and p160) to form structural proteins of the virion core (i.e., p17, p24, p9, and p7) and essential viral enzymes (i.e., reverse transcriptase, integrase, and protease). By interfering with the formation of these essential proteins and enzymes, ritonavir blocks maturation of the virus and causes formation of nonfunctional, immature, noninfectious virions. Ritonavir is active in both acutely and chronically infected cells since it targets the HIV replication cycle after translation and before assembly. Thus, the drug is active in chronically infected cells (e.g., monocytes and macrophages) that generally are not affected by nucleoside reverse transcriptase inhibitors (e.g., didanosine, lamivudine, stavudine, zalcitabine, zidovudine). Ritonavir does not affect early stages of the HIV replication cycle; however, the drug interferes with production of infectious HIV and limits further infectious spread of the virus. While the complete mechanisms of antiviral activity of ritonavir have not been fully elucidated, ritonavir apparently inhibits replication of retroviruses, including human immunodeficiency virus type 1 (HIV-1) and 2 (HIV-2), by interfering with HIV protease. The drug, therefore, exerts a virustatic effect against retroviruses by acting as an HIV protease inhibitor.

Pharmacodynamics

Ritonavir is a protease inhibitor with activity against Human Immunodeficiency Virus Type 1 (HIV-1). Protease inhibitors block the part of HIV called protease. HIV-1 protease is an enzyme required for the proteolytic cleavage of the viral polyprotein precursors into the individual functional proteins found in infectious HIV-1. Ritonavir binds to the protease active site and inhibits the activity of the enzyme. This inhibition prevents cleavage of the viral polyproteins resulting in the formation of immature non-infectious viral particles. Protease inhibitors are almost always used in combination with at least two other anti-HIV drugs. Modern protease inhibitors require the use of low-dose ritonavir to boost pharmacokinetic exposure through inhibition of metabolism via the cytochrome P450 3A4 enzyme pathway.