Tafluprost (trade names Taflotan by
Santen Pharmaceutical, Zioptan by Merck in the US and Saflutan by Mundipharma in Australia) is a
prostaglandin analogue. It is used topically (as
eye drops) to control the progression of
open-angle glaucoma and in the management of
ocular hypertension, alone or in combination with other medication. It reduces
intraocular pressure by increasing the outflow of
aqueous fluid from the eyes.
Adverse effects
The most common side effect is
conjunctival hyperemia, which occurs in 4 to 20% of patients. Less common side effects include stinging of the eyes, headache, and
respiratory infections. Rare side effects are
dyspnoea (breathing difficulties), worsening of
asthma, and
macular oedema
Macular edema occurs when fluid and protein deposits collect on or under the macula of the eye (a yellow central area of the retina) and causes it to thicken and swell ( edema). The swelling may distort a person's central vision, because the macu ...
.
Interactions
Nonsteroidal anti-inflammatory drug
Non-steroidal anti-inflammatory drugs (NSAID) are members of a therapeutic drug class which reduces pain, decreases inflammation, decreases fever, and prevents blood clots. Side effects depend on the specific drug, its dose and duration of ...
s (NSAIDs) can either reduce or increase the effect of tafluprost.
Timolol eye drops, a common kind of glaucoma medication, does not negatively interact with this drug.
No interactions with systemic (for example, oral) drugs are expected because tafluprost does not reach relevant concentrations in the bloodstream.
Pharmacology
Mechanism of action
Tafluprost is a
prodrug
A prodrug is a medication or compound that, after intake, is metabolized (i.e., converted within the body) into a pharmacologically active drug. Instead of administering a drug directly, a corresponding prodrug can be used to improve how the drug ...
of the active substance, tafluprost acid, a
structural and
functional analogue of
prostaglandin F2α (PGF
2α). Tafluprost acid is a selective
agonist
An agonist is a chemical that activates a receptor to produce a biological response. Receptors are cellular proteins whose activation causes the cell to modify what it is currently doing. In contrast, an antagonist blocks the action of the ago ...
at the
prostaglandin F receptor, increasing outflow of aqueous fluid from the eyes and thus lowering intraocular pressure.
Other PGF
2α analogues with the same mechanism include
latanoprost and
travoprost.
Pharmacokinetics
Tafluprost, as a
lipophilic ester, easily penetrates the
cornea and is then activated to the
carboxylic acid
In organic chemistry, a carboxylic acid is an organic acid that contains a carboxyl group () attached to an R-group. The general formula of a carboxylic acid is or , with R referring to the alkyl, alkenyl, aryl, or other group. Carboxylic ...
, tafluprost acid. Onset of action is 2 to 4 hours after application, the maximal effect is reached after 12 hours, and ocular pressure remains lowered for at least 24 hours.
Tafluprost acid is inactivated by
beta oxidation to 1,2-dinortafluprost acid, 1,2,3,4-tetranortafluprost acid, and its
lactone, which are subsequently
glucuronidated or
hydroxylated
In chemistry, hydroxylation can refer to:
*(i) most commonly, hydroxylation describes a chemistry, chemical process that introduces a hydroxyl group () into an organic compound.
*(ii) the ''degree of hydroxylation'' refers to the number of OH gr ...
. The
cytochrome P450
Cytochromes P450 (CYPs) are a Protein superfamily, superfamily of enzymes containing heme as a cofactor (biochemistry), cofactor that functions as monooxygenases. In mammals, these proteins oxidize steroids, fatty acids, and xenobiotics, and are ...
liver enzymes play no role in the metabolism.
An analogous pathway (at least up to the tetranor-metabolites) has been found for latanoprost and travoprost.
References
{{Prostanoidergics
Prostaglandins
Secondary alcohols
Alkene derivatives
Merck & Co. brands
Carboxylate esters
Isopropyl esters
Organofluorides
Phenol ethers
Ophthalmology drugs