Peringatan Keamanan

Symptoms of overdose include vomiting, agitation, tremors, hyperreflexia, muscle twitching, convulsions (may be followed by coma), euphoria, confusion, hallucinations, delirium, sweating, flushing, headache, hyperpyrexia, tachycardia, palpitations, cardiac arrhythmias, hypertension, mydriasis, and dryness of mucous membranes. LD50=190mg/kg (orally in mice)

Methylphenidate

DB00422

small molecule approved investigational

Deskripsi

Methylphenidate is a central nervous system stimulant used most commonly in the treatment of Attention-Deficit/Hyperactivity Disorder (ADHD) and for narcolepsy. Also known as the marketed products Ritalin, Concerta, or Biphentin, methylphenidate is used with other treatment modalities (psychological, educational, cognitive behaviour therapy, etc) to improve the following group of developmentally inappropriate symptoms associated with ADHD: moderate-to-severe distractibility, short attention span, hyperactivity, emotional lability, and impulsivity. Long-acting formulations of psychostimulants such as methylphenidate, DB01576, and DB01255 are considered the most effective and widely used treatment for ADHD, and are considered first-line options for children, adolescents, and adults as recommended by CADDRA (Canadian ADHD Resource Alliance). L6037 CADDRA recommends the use of methylphenidate due to long term studies, of over twenty years in duration, which show methylphenidate is safe and effective.

While its exact mechanism is unclear, methylphenidate (MPH) has been shown to act as a norepinephrine and dopamine reuptake inhibitor (NDRI), thereby increasing the presence of these neurotransmitters in the extraneuronal space and prolonging their action.A177541 There is a dose-related effect of psychostimulants on receptor stimulation, where higher doses are shown to increase norepinephrine (NE) and dopamine (DA) efflux throughout the brain which can result in impaired cognition and locomotor-activating effects. In contrast, low doses are found to selectively activate NE and DA neurotransmission within the prefrontal cortex which is an area of the brain thought to play a prominent role in ADHD pathophysiology, thereby improving clinical efficacy and preventing side effects.A177547 The lower doses used to treat ADHD are not associated with the locomotor-activating effects associated with higher doses and instead reduce movement, impulsivity, and increase cognitive function including sustained attention and working memory.A177541, A177544 Methylphenidate's beneficial effects in sustaining attention have also been shown to be mediated by alpha-1 adrenergic receptor activity.A177550 Clinical findings have shown that children with ADHD have an abnormality in the dopamine transporter gene (DAT1), the D4 receptor gene (DRD-4), and/or the D2 receptor gene that may be at least partly overcome by the dopaminergic effects of methylphenidate, suggesting a possible mode of action.F4474

When provided as Biphentin®, methylphenidate is released through a multi-layer release delivery system (MLRTM) where 40% of the dose is provided as an immediate release and 60% is provided through a gradual release. Biphentin was designed to be an alternative to separate doses of immediate-release (IR) methylphenidate by providing a biphasic concentration-time profile when given as a single dose. The MLRTM release system allows for a sustained effect for 10-12 hours, allowing for once-daily dosing that covers the major times that ADHD impairment might occur (such as school, homework periods, during the work day, etc).

When provided as Concerta®, methylphenidate is released through the patented Osmotic Controlled-Release Oral Delivery (OROS) system where 22% of the dose is provided as an immediate release and 78% is provided through a gradual release.A631 OROS is comprised of an osmotically active trilayer core surrounded by a semipermeable membrane with an immediate-release drug overcoat. Within an aqueous environment, such as the stomach, the drug overcoat, which consists of 22% of the dose, dissolves within one hour, providing an initial immediate-release formulation of methylphenidate. Water then permeates through the membrane into the tablet core where the osmotically active polymer excipients expand, allowing methylphenidate to release slowly through the orifice over a period of 6-7 hours. Concerta also provides a sustained 10-12 hour effect, allowing for once-daily dosing.

Methylphenidate contains a blackbox warning stating that CNS stimulants, including methylphenidate-containing products and amphetamines, have a high potential for abuse and dependence. This abuse potential is likely related to the effects associated with higher doses of methylphenidate, which induce surface expression of the dopamine transporter (DAT).A177553 In particular, increased dopamine in key brain areas is associated with the reinforcing and addictive properties of psychostimulants such as methylphenidate, and even amplifies the potency and reinforcing effects of other drugs of abuse such as amphetamines, making ADHD sufferers more susceptible to their addictive effects.A177556 Concerns about abuse potential have spurred research into medications with fewer effects on DAT and the use of non-stimulant ADHD medications including DB00289 and DB01018.

Struktur Molekul 2D

Berat 233.3062
Wujud solid

Peta Jejaring Molekuler
Legenda: ObatTargetGenEnzim(Panah → menunjukkan arah efek / relasi)TransporterCarrier

Profil Farmakokinetik

Waktu Paruh (Half-Life) Concerta: The half-life of methylphenidate in adults following oral administration of Concerta® was approximately 3.5 h.[F4474] Biphentin: Methylphenidate is eliminated from plasma with a mean half-life of 2.4 hours in children and 2.1 hours in adults.[F4480] Methylphenidate (immediate release): Methylphenidate is eliminated from the plasma with a mean half-life of 2.4 hours in children and 2.1 hours in adults.[F4483]
Volume Distribusi Concerta: Plasma methylphenidate concentrations in adults decline bi-exponentially following oral administration.[F4474] Biphentin: The apparent distribution volume of methylphenidate in children is approximately 20 L/kg, with substantial variability (11 to 33 L/kg).[F4480] Methylphenidate (immediate release): The apparent distribution volume of methylphenidate in children was approximately 20 L/kg, with substantial variability (11-33 L/kg). The volume of distribution after an intravenous dose (Vss) is 2.23 L/kg for the racemate in healthy adult volunteers.[F4483]
Klirens (Clearance) The apparent mean systemic clearance after an oral dose is 10.2 and 10.5 L/h/kg in children and adults, respectively for a 0.3 mg/kg dose, and 0.565 L/h/kg after an intravenous dose of the racemate in healthy adult volunteers.[F4483]

Absorpsi

Concerta®: Methylphenidate is readily absorbed. Following oral administration of Concerta, plasma methylhphenidate concentrations reach an initial maximum at about 1 hour followed by gradual ascending concentrations over the next 5-9 hours. Mean times to reach peak plasma concentrations across all doses of Concerta occurred between 6-10 hours. Once daily dosing minimizes the fluctuations between peak and trough concentrations associated with multiple doses of immediate-release methylphenidate treatments.F4474 Depending on the doses provided, Cmax was found to range from 6.0-15.0ng/mL, Tmax ranged from 8.1-9.4h, and AUC ranged from 50.4-121.5 ng·h/mL in children.F4474 When provided as Concerta®, methylphenidate is released through the patented Osmotic Controlled-Release Oral Delivery (OROS) system where 22% of the dose is provided as an immediate release and 78% is provided through a gradual release.A631 OROS is comprised of an osmotically active trilayer core surrounded by a semipermeable membrane with an immediate-release drug overcoat. Within an aqueous environment, such as the stomach, the drug overcoat, which consists of 22% of the dose, dissolves within one hour, providing an initial immediate-release formulation of methylphenidate. Water then permeates through the membrane into the tablet core where the osmotically active polymer excipients expand, allowing methylphenidate to release slowly through the orifice over a period of 6-7 hours. Concerta also provides a sustained 10-12 hour effect, allowing for once-daily dosing. Biphentin®: Methylphenidate is rapidly and extensively absorbed following oral administration, with peak blood levels obtained in 1-3 hours.F4480 When provided as Biphentin®, methylphenidate is released through a multi-layer release delivery system (MLRTM) where 40% of the dose is provided as an immediate release and 60% is provided through a gradual release. Biphentin was designed to be an alternative to separate doses of immediate-release (IR) methylphenidate by providing a biphasic concentration-time profile when given as a single dose. The MLRTM release system allows for a sustained effect for 10-12 hours, allowing for once-daily dosing that covers the major times that ADHD impairment might occur (such as school, homework periods, during the workday, etc). Methylphenidate (immediate release): Methylphenidate hydrochloride is rapidly and extensively absorbed from the tablets following oral administration; however, owing to extensive first-pass metabolism, bioavailability is low (approx. 30%) and large individual differences exist (11-52%). In one study, the administration of methylphenidate hydrochloride with food accelerated absorption but had no effect on the amount absorbed. Peak plasma concentrations of 10.8 and 7.8 ng/mL were observed, on average, 2 hours after administration of 0.30 mg/kg in children and adults, respectively. Peak plasma concentrations showed marked variability between subjects. Both the area under the concentration-time curve (AUC), and the peak plasma concentrations (Cmax) showed dose-proportionality.F4483

Metabolisme

Methylphenidate is hepatically metabolized. More specifically, it is rapidly and extensively metabolized by carboxylesterase CES1A1. Via this enzyme, methylphenidate undergoes de-esterification to ritalinic acid (a-phenyl-2-piperidine acetic acid, PPAA), which has little to no pharmacologic activity.

Rute Eliminasi

After oral administration of an immediate release formulation of methylphenidate, 78%-97% of the dose is excreted in the urine and 1%-3% in the feces in the form of metabolites within 48-96 hours. Only small quantities (<1%) of unchanged methylphenidate appear in the urine. Most of the dose is excreted in the urine as ritalinic acid (60%-86%), the remainder being accounted for by minor metabolites.

Interaksi Makanan

2 Data
  • 1. Avoid alcohol. Co-administration with alcohol may cause a "dose-dumping" effect with some extended-release formulations of methylphenidate. It may also potentiate the CNS effects of methylphenidate.
  • 2. Take with or without food. Patients may take methylphenidate with food to alleviate GI upset.

Interaksi Obat

782 Data
Valsartan Methylphenidate may decrease the antihypertensive activities of Valsartan.
Ramipril Methylphenidate may decrease the antihypertensive activities of Ramipril.
Esmolol Methylphenidate may decrease the antihypertensive activities of Esmolol.
Betaxolol Methylphenidate may decrease the antihypertensive activities of Betaxolol.
Reserpine Methylphenidate may decrease the antihypertensive activities of Reserpine.
Remikiren Methylphenidate may decrease the antihypertensive activities of Remikiren.
Torasemide Methylphenidate may decrease the antihypertensive activities of Torasemide.
Bethanidine Methylphenidate may decrease the antihypertensive activities of Bethanidine.
Guanadrel Methylphenidate may decrease the antihypertensive activities of Guanadrel.
Metoprolol Methylphenidate may decrease the antihypertensive activities of Metoprolol.
Isradipine Methylphenidate may decrease the antihypertensive activities of Isradipine.
Olmesartan Methylphenidate may decrease the antihypertensive activities of Olmesartan.
Chlorthalidone Methylphenidate may decrease the antihypertensive activities of Chlorthalidone.
Nitroprusside Methylphenidate may decrease the antihypertensive activities of Nitroprusside.
Atenolol Methylphenidate may decrease the antihypertensive activities of Atenolol.
Diltiazem Methylphenidate may decrease the antihypertensive activities of Diltiazem.
Minoxidil Methylphenidate may decrease the antihypertensive activities of Minoxidil.
Timolol Methylphenidate may decrease the antihypertensive activities of Timolol.
Treprostinil Methylphenidate may decrease the antihypertensive activities of Treprostinil.
Amlodipine Methylphenidate may decrease the antihypertensive activities of Amlodipine.
Nimodipine Methylphenidate may decrease the antihypertensive activities of Nimodipine.
Nisoldipine Methylphenidate may decrease the antihypertensive activities of Nisoldipine.
Bendroflumethiazide Methylphenidate may decrease the antihypertensive activities of Bendroflumethiazide.
Prazosin Methylphenidate may decrease the antihypertensive activities of Prazosin.
Fosinopril Methylphenidate may decrease the antihypertensive activities of Fosinopril.
Trandolapril Methylphenidate may decrease the antihypertensive activities of Trandolapril.
Metolazone Methylphenidate may decrease the antihypertensive activities of Metolazone.
Lercanidipine Methylphenidate may decrease the antihypertensive activities of Lercanidipine.
Benazepril Methylphenidate may decrease the antihypertensive activities of Benazepril.
Bosentan Methylphenidate may decrease the antihypertensive activities of Bosentan.
Propranolol Methylphenidate may decrease the antihypertensive activities of Propranolol.
Enalapril Methylphenidate may decrease the antihypertensive activities of Enalapril.
Doxazosin Methylphenidate may decrease the antihypertensive activities of Doxazosin.
Labetalol Methylphenidate may decrease the antihypertensive activities of Labetalol.
Cyclothiazide Methylphenidate may decrease the antihypertensive activities of Cyclothiazide.
Bisoprolol Methylphenidate may decrease the antihypertensive activities of Bisoprolol.
Candoxatril Methylphenidate may decrease the antihypertensive activities of Candoxatril.
Nicardipine Methylphenidate may decrease the antihypertensive activities of Nicardipine.
Guanabenz Methylphenidate may decrease the antihypertensive activities of Guanabenz.
Mecamylamine Methylphenidate may decrease the antihypertensive activities of Mecamylamine.
Losartan Methylphenidate may decrease the antihypertensive activities of Losartan.
Moexipril Methylphenidate may decrease the antihypertensive activities of Moexipril.
Phentolamine Methylphenidate may decrease the antihypertensive activities of Phentolamine.
Eplerenone Methylphenidate may decrease the antihypertensive activities of Eplerenone.
Lisinopril Methylphenidate may decrease the antihypertensive activities of Lisinopril.
Nitroglycerin Methylphenidate may decrease the antihypertensive activities of Nitroglycerin.
Metyrosine Methylphenidate may decrease the antihypertensive activities of Metyrosine.
Hydroflumethiazide Methylphenidate may decrease the antihypertensive activities of Hydroflumethiazide.
Cryptenamine Methylphenidate may decrease the antihypertensive activities of Cryptenamine.
Perindopril Methylphenidate may decrease the antihypertensive activities of Perindopril.
Candesartan cilexetil Methylphenidate may decrease the antihypertensive activities of Candesartan cilexetil.
Tolazoline Methylphenidate may decrease the antihypertensive activities of Tolazoline.
Fenoldopam Methylphenidate may decrease the antihypertensive activities of Fenoldopam.
Indapamide Methylphenidate may decrease the antihypertensive activities of Indapamide.
Tadalafil Methylphenidate may decrease the antihypertensive activities of Tadalafil.
Alprenolol Methylphenidate may decrease the antihypertensive activities of Alprenolol.
Eprosartan Methylphenidate may decrease the antihypertensive activities of Eprosartan.
Chlorothiazide Methylphenidate may decrease the antihypertensive activities of Chlorothiazide.
Quinapril Methylphenidate may decrease the antihypertensive activities of Quinapril.
Omapatrilat Methylphenidate may decrease the antihypertensive activities of Omapatrilat.
Phenoxybenzamine Methylphenidate may decrease the antihypertensive activities of Phenoxybenzamine.
Pindolol Methylphenidate may decrease the antihypertensive activities of Pindolol.
Telmisartan Methylphenidate may decrease the antihypertensive activities of Telmisartan.
Methyldopa Methylphenidate may decrease the antihypertensive activities of Methyldopa.
Hydrochlorothiazide Methylphenidate may decrease the antihypertensive activities of Hydrochlorothiazide.
Guanfacine Methylphenidate may decrease the antihypertensive activities of Guanfacine.
Trichlormethiazide Methylphenidate may decrease the antihypertensive activities of Trichlormethiazide.
Felodipine Methylphenidate may decrease the antihypertensive activities of Felodipine.
Irbesartan Methylphenidate may decrease the antihypertensive activities of Irbesartan.
Nitrendipine Methylphenidate may decrease the antihypertensive activities of Nitrendipine.
Deserpidine Methylphenidate may decrease the antihypertensive activities of Deserpidine.
Pentolinium Methylphenidate may decrease the antihypertensive activities of Pentolinium.
Trimethaphan Methylphenidate may decrease the antihypertensive activities of Trimethaphan.
Diazoxide Methylphenidate may decrease the antihypertensive activities of Diazoxide.
Carvedilol Methylphenidate may decrease the antihypertensive activities of Carvedilol.
Bretylium Methylphenidate may decrease the antihypertensive activities of Bretylium.
Terazosin Methylphenidate may decrease the antihypertensive activities of Terazosin.
Guanethidine Methylphenidate may decrease the antihypertensive activities of Guanethidine.
Rescinnamine Methylphenidate may decrease the antihypertensive activities of Rescinnamine.
Acebutolol Methylphenidate may decrease the antihypertensive activities of Acebutolol.
Captopril Methylphenidate may decrease the antihypertensive activities of Captopril.
Nadolol Methylphenidate may decrease the antihypertensive activities of Nadolol.
Epoprostenol Methylphenidate may decrease the antihypertensive activities of Epoprostenol.
Bepridil Methylphenidate may decrease the antihypertensive activities of Bepridil.
Hydralazine Methylphenidate may decrease the antihypertensive activities of Hydralazine.
Bevantolol Methylphenidate may decrease the antihypertensive activities of Bevantolol.
Practolol Methylphenidate may decrease the antihypertensive activities of Practolol.
Polythiazide Methylphenidate may decrease the antihypertensive activities of Polythiazide.
Cilazapril Methylphenidate may decrease the antihypertensive activities of Cilazapril.
Saprisartan Methylphenidate may decrease the antihypertensive activities of Saprisartan.
Spirapril Methylphenidate may decrease the antihypertensive activities of Spirapril.
Penbutolol Methylphenidate may decrease the antihypertensive activities of Penbutolol.
Mibefradil Methylphenidate may decrease the antihypertensive activities of Mibefradil.
Oxprenolol Methylphenidate may decrease the antihypertensive activities of Oxprenolol.
Dexpropranolol Methylphenidate may decrease the antihypertensive activities of Dexpropranolol.
Tienilic acid Methylphenidate may decrease the antihypertensive activities of Tienilic acid.
Debrisoquine Methylphenidate may decrease the antihypertensive activities of Debrisoquine.
Celiprolol Methylphenidate may decrease the antihypertensive activities of Celiprolol.
Nebivolol Methylphenidate may decrease the antihypertensive activities of Nebivolol.
Lofexidine Methylphenidate may decrease the antihypertensive activities of Lofexidine.

Target Protein

Sodium-dependent dopamine transporter SLC6A3
5-hydroxytryptamine receptor 1A HTR1A
Sodium-dependent noradrenaline transporter SLC6A2

Referensi & Sumber

Artikel (PubMed)
  • PMID: 11524026
    Keating GM, McClellan K, Jarvis B: Methylphenidate (OROS formulation). CNS Drugs. 2001;15(6):495-500; discussion 501-3.
  • PMID: 17201613
    Markowitz JS, DeVane CL, Pestreich LK, Patrick KS, Muniz R: A comprehensive in vitro screening of d-, l-, and dl-threo-methylphenidate: an exploratory study. J Child Adolesc Psychopharmacol. 2006 Dec;16(6):687-98.
  • PMID: 15661631
    Fone KC, Nutt DJ: Stimulants: use and abuse in the treatment of attention deficit hyperactivity disorder. Curr Opin Pharmacol. 2005 Feb;5(1):87-93.
  • PMID: 2190251
    Sharma RP, Javaid JI, Pandey GN, Easton M, Davis JM: Pharmacological effects of methylphenidate on plasma homovanillic acid and growth hormone. Psychiatry Res. 1990 Apr;32(1):9-17.
  • PMID: 22763750
    Hodgkins P, Shaw M, Coghill D, Hechtman L: Amfetamine and methylphenidate medications for attention-deficit/hyperactivity disorder: complementary treatment options. Eur Child Adolesc Psychiatry. 2012 Sep;21(9):477-92. doi: 10.1007/s00787-012-0286-5. Epub 2012 Jul 5.
  • PMID: 16806100
    Berridge CW, Devilbiss DM, Andrzejewski ME, Arnsten AF, Kelley AE, Schmeichel B, Hamilton C, Spencer RC: Methylphenidate preferentially increases catecholamine neurotransmission within the prefrontal cortex at low doses that enhance cognitive function. Biol Psychiatry. 2006 Nov 15;60(10):1111-20. doi: 10.1016/j.biopsych.2006.04.022. Epub 2006 Jun 23.
  • PMID: 9708845
    Solanto MV: Neuropsychopharmacological mechanisms of stimulant drug action in attention-deficit hyperactivity disorder: a review and integration. Behav Brain Res. 1998 Jul;94(1):127-52.
  • PMID: 18591484
    Brennan AR, Arnsten AF: Neuronal mechanisms underlying attention deficit hyperactivity disorder: the influence of arousal on prefrontal cortical function. Ann N Y Acad Sci. 2008;1129:236-45. doi: 10.1196/annals.1417.007.
Menampilkan 8 dari 11 artikel.

Contoh Produk & Brand

Produk: 634 • International brands: 5
Produk
  • Act Methylphenidate ER
    Tablet, extended release • 18 mg • Oral • Canada • Approved
  • Act Methylphenidate ER
    Tablet, extended release • 27 mg • Oral • Canada • Approved
  • Act Methylphenidate ER
    Tablet, extended release • 36 mg • Oral • Canada • Approved
  • Act Methylphenidate ER
    Tablet, extended release • 54 mg • Oral • Canada • Approved
  • Adhansia XR
    Capsule, extended release • 25 mg/1 • Oral • US • Approved
  • Adhansia XR
    Capsule, extended release • 35 mg/1 • Oral • US • Approved
  • Adhansia XR
    Capsule, extended release • 45 mg/1 • Oral • US • Approved
  • Adhansia XR
    Capsule, extended release • 55 mg/1 • Oral • US • Approved
Menampilkan 8 dari 634 produk.
International Brands
  • Equasym XL
  • Medikinet XL
  • Quillivant
  • Riphenidate
  • Rubifen SR

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