Pentosan polysulfate
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| Clinical data |
| AHFS/Drugs.com |
Consumer Drug Information |
Pregnancy
category |
|
Routes of
administration |
Oral, intramuscular, intra-articular, intraventricular |
| Pharmacokinetic data |
| Excretion |
Urine |
| Identifiers |
| CAS Number |
37300-21-3 Y (free acid)
116001-96-8 (sodium salt) |
| ATC code |
C05BA04 (WHO) G04BX15 (WHO) QM01AX90 (WHO) |
| PubChem |
CID 37720 |
| ChemSpider |
none |
| ChEMBL |
CHEMBL1201516 |
| Chemical data |
| Formula |
(C5H6Na2O10S2)n |
| (verify) |
Pentosan polysulfate (PPS, (1->4)-β-Xylan 2,3-bis(hydrogen sulfate) with a 4 O-methyl-α-D-glucuronate) is a semi-synthetic polysulfated xylan sold for the relief of various medical conditions including thrombi and interstitial cystitis in humans and osteoarthritis in dogs and horses. Various brand names for the human drug include Elmiron (as sodium salt), Hemoclar, Anarthron, Fibrase, Thrombocid and SP54. PPS Capsule is sold as Pentossan-100 by Molclone Labs India. PPS is also sold under the brand name Comfora in India. In the veterinary field, pentosan polysulfate is sold as Cartrophen Vet and Sylvet by Biopharm Australia, and Pentosan by Naturevet Australia.
The calcium salt of PPS was one of the first reported disease-modifying osteoarthritis drugs (DMOAD).[1]
Contents
- 1 Medical uses
- 1.1 Anticoagulation
- 1.2 Interstitial cystitis/painful bladder syndrome
- 1.3 Osteoarthritis/degenerative joint disease
- 1.3.1 Canines
- 1.3.2 Horses
- 1.3.3 Humans
- 1.4 Transmissible spongiform encephalopathies
- 2 Adverse effects
- 3 References
- 4 External links
Medical uses
Anticoagulation
The anticoagulant activity of PPS is 1/15 that of heparin. PPS acts by binding to thrombin, thus interfering with the binding of thrombin to antithrombin III.[2]
Interstitial cystitis/painful bladder syndrome
Interstitial cystitis/painful bladder syndrome (IC/PBS) is a condition where patients struggle with symptoms of urinary frequency, urgency, pressure and/or pain, as well as nocturia (frequent urination at night), dyspareunia (painful intercourse), pain and/or discomfort while sitting in a car, while driving and/or traveling. PPS, as Elmiron, is the only oral medication approved by the U.S. Food and Drug Administration (FDA) for the treatment of IC. Elmiron is available as pills or as a direct infusion into the bladder. A review of four placebo-controlled studies concluded that that PPS was significantly more effective than placebo for pain, urgency and frequency of urination, but not different from placebo for nocturia (needing to urinate during the night).[3]
In IC, PPS is believed to work by providing a protective coating to the damaged bladder wall. PPS is similar in structure to the natural glycosaminoglycan coating of the inner lining of the bladder, and may replace or repair the lining, reducing its permeability.[4] This lining is important in preventing urinary toxins from irritating the underlying cell layers. Evidence for this mechanism was found by irritating the lining of the bladders of female rats with acrolein. If the rats were pre-treated with PPS, the damage was much less.[5] Potassium sensitivity tests (PST) showed abnormal cell lining permeability in most patients with IC and indicated a significant reduction in permeability after successful PPS therapy (32-week trial of 300, 600, or 900 mg PPS/day).[6] Another possible mechanism of PPS action in IC is by inhibiting the inflammatory response of the bladder cells, either by indirectly blocking the activity of mediators such as NF-κB,[7] by preventing an influx of mast cells [8] or by preventing mast cells releasing histamine.[9]
The sodium salt of PPS has low bioavailability when taken orally. Research presented in 2005 by Alza Pharmaceuticals demonstrated that 94% of the medication was excreted, intact, in faeces.[10] This means that 6% was excreted through urine and in contact with the bladder. The drug appears to be most effective when taken for several months. More recently, PPS has been studied as part of a "rescue instillation" which is placed directly in the bladder and can, perhaps, provide better effectiveness. Research presented in 2005 showed PPS had 90% effectiveness in reducing the symptoms of IC/PBS patients by using this instillation.[11]
Osteoarthritis/degenerative joint disease
PPS was first reported as a chondroprotective drug in 1988 [12] with a detailed rationale of the disease-modifying activity of this molecule subsequently published in 1999.[13] The mechanism of PPS action in osteoarthritis is multifactorial, with both stimulation of cartilage matrix synthesis and prevention of cartilage breakdown. There are also systemic effects on blood lipids and fibrinolysis that may help clear the subchondral circulation. Calcium pentosan polysulfate (CaPPS) was shown to be absorbed better when taken orally than the sodium salt [14] and maintained the proteoglycan content in the articular cartilage in experimentally inflamed rabbit joints.[15]
Diagram represents the osteoarthritis cycle with reference to PPS site of action
Canines
Read et al. (1996) [16] used three different doses of sodium PPS to treat 40 geriatric dogs with well-established clinical signs of chronic OA with SC injection. The 3 mg/kg dose was the most effective. In a study conducted with 10 elderly dogs with osteoarthritis given calcium PPS (3 mg/kg intramuscularly) once weekly for four weeks, the improvement in symptoms (seen at 1, 2, 3 and 7 weeks after initiation of therapy) was found to correlate with plasma indices of fibrinolytic activity and lipid profiles.[17] In a study in dogs with OA secondary to cranial cruciate ligament (CCL) deficiency, although no differences were identified in either functional outcome or radiographic progression using the oral calcium PPS compared with placebo, there were significantly lower levels of proteoglycan breakdown products in the synovial fluid of the osteoarthritic joints.[18] The efficacy of subcutaneous sodium PPS (3 mg/kg) was tested in 40 dogs with cranial cruciate ligament (CCL) instability and found to hasten recovery, as measured by more rapidly improved ground reaction forces (GRF), over 48 weeks.[19]
Horses
There are few published reports describing the use of PPS for equine joint disease, however the drug is being used for this indication in Australia. When administered to racing Thoroughbreds with chronic osteoarthritis (2 to 3 mg/kg, intramuscularly, once weekly for 4 weeks, then as required), PPS treatment improved but did not eliminate clinical signs of joint disease.[20] Articular cartilage fibrillation was substantially reduced by similar NaPPS treatment intramuscularly in nine horse with experimentally-induced carpal osteoarthritis.[21] Despite limited published studies on the effect of PPS in horses, most surveyed owners and trainers in Australia found the intramuscular PPS treatment to be highly efficacious when used as a prophylactic prior to competition.[22]
Humans
After a series of four to six intra-articular PPS injections into knees of human volunteers, there was a significant increase in the size of the synovial fluid hyaluronan without causing any inflammation or bleeding into the joint cavity.[23] Preliminary reports of an open study of 23 patients with mild to moderate OA of the hand, hip, or knee, found that CaPPS (2 mg/kg intramuscularly once a week for 5 weeks) provided relief of symptoms and normalised hematologic parameters of coagulation and thrombolysis.[24] Another preliminary report described the first 31 of 86 patients with OA of the knee who were subjected to intra-articular sodium PPS injections (n=15) compared to an equivalent volume of IA Ringer's solution (n=16) under double-blind conditions.[25] NaPPS was significantly better than placebo for patient stiffness, walking on a level surface and pain in the previous 48 hours and previous month for multiple time points after treatment. The patients who had intra-articular PPS injections had synovial fluid with significantly better viscoelasticity (lubricating properties) due to significantly higher molecular weight hyaluronan.[26]
When eleven women with knee or hip OA were injected with 3 mg/kg NaPPS, both hepatolipases and lipoprotein lipases were significantly elevated in their plasma for at least eight hours but had returned to normal levels by 24 hours.[13] A double blind, placebo-controlled clinical study in 114 patients with osteoarthritis of the knee was performed in Perth, Australia where patients either received a salt solution or sodium PPS at 3 mg/ kg as an intramuscular injection once weekly for 4 weeks.[27] Overall, NaPPS treatment significantly improved the duration of joint stiffness and pain at rest compared with controls for 20 weeks after the cessation of treatment, and significantly improved pain on walking and overall function for 8 weeks after the cessation of treatment. Twenty patients with knee OA were assessed clinically at Nagasaki University Hospital in a single-center, open-label trial. Treatment consisted of 6 weekly subcutaneous injections of pentosan (2 mg/kg). Knee flexion, pain while walking, pain after climbing up and down stairs were improved significantly for up to a year.[28]
Transmissible spongiform encephalopathies
PPS gained attention as possibly being effective in the treatment of Creutzfeldt-Jakob disease (CJD). The rationale for this treatment was unclear but it was subsequently shown in prion-infected mouse neuroblastoma cells that PPS could rapidly reduce the levels of abnormal (scrapie) prion without affecting the normal cellular isoform.[29] As PPS can bind to the cellular isoform of the prion protein, it may stabilise this form and prevent its conversion to the pathological (scrapie) isoform.[30]
The treatment[31] of one patient in Northern Ireland and around six other patients in mainland Britain were reported in the press.[32] No patients showed signs of clinical improvement, however the disease was very advanced when the therapy was initiated.
Around 15 other patients in non-UK countries have also received this PPS treatment in an attempt to halt or slow down CJD and related disease progression. There are also clinical trials of Elmiron to treat Hunters Syndrome (MPS II).
Adverse effects
Patients who have taken PPS orally report a variety of side effects, primarily gastrointestinal complaints such as diarrhea, heartburn, and stomach pain.[33] Hair loss, headache, rash, and insomnia have also been reported.[33] Due to Elmiron's anticoagulant effects, some patients report bruising more easily. In some cases, patients are asked to stop taking the medication before any major surgical procedures to reduce the likelihood of bleeding.
References
- ^ Ghosh, P; Smith, M (2002). "Osteoarthritis, genetic and molecular mechanisms". Biogerontology 3 (1-2): 85–8. doi:10.1023/a:1015219716583. PMID 12014849.
- ^ Scully, MF; Kakkar, vv (1984). "The antiheparin effect of a heparinoid, pentosan polysulphate". Biochem J 218: 657–665. doi:10.1042/bj2180657. PMID 6202294.
- ^ Hwang P, Auclair B, Beechinor D, Diment M, Einarson TR (July 1997). "Efficacy of pentosan polysulfate in the treatment of interstitial cystitis: a meta-analysis". Urology 50 (1): 39–43. doi:10.1016/S0090-4295(97)00110-6. PMID 9218016.
- ^ Parsons CL (1994). "The therapeutic role of sulfated polysaccharides in the urinary bladder". Urol Clin North Am 21 (1): 93–100. PMID 7904388.
- ^ Kalota SJ, Stein PC, Parsons CL (1992). "Prevention of acrolein-induced bladder injury by pentosanpolysulfate". J Urol 148 (1): 163–166. PMID 1377288.
- ^ Parsons CL, Forrest J, Nickel JC, Evans R, Lloyd LK, Barkin J, Mosbaugh PG, Kaufman DM, Hernandez-Graulau JM, Atkinson L, Albrecht D; Elmiron Study Group. (2002). "<Effect of pentosan polysulfate therapy on intravesical potassium sensitivity". Urology 59 (3): 329–333. doi:10.1016/s0090-4295(01)01586-2. PMID 11880064.
- ^ Sadhukhan PC, Tchetgen MB, Rackley RR, Vasavada SP, Liou L, Bandyopadhyay SK (2002). "Sodium pentosan polysulfate reduces urothelial responses to inflammatory stimuli via an indirect mechanism". J Urol 168 (1): 289–292. doi:10.1016/s0022-5347(05)64909-9. PMID 12050558.
- ^ Chiang G, Patra P, Letourneau R, Jeudy S, Boucher W, Green M, Sant GR, Theoharides TC (2002). "Pentosanpolysulfate inhibits mast cell histamine secretion and intracellular calcium ion levels: an alternative explanation of its beneficial effect in interstitial cystitis". J Urol 164 (6): 2119–2125. doi:10.1016/s0022-5347(05)66981-9. PMID 11061939.
- ^ Chiang G, Patra P, Letourneau R, Jeudy S, Boucher W, Green M, Sant GR, Theoharides TC (2003). "Pentosanpolysulfate (Elmiron) is a potent inhibitor of mast cell histamine secretion". Adv Exp Med Biol 539 (Pt B): 713–729. PMID 15176320.
- ^ Simon, M; McClanahan, RH; Shah, JF; et al. (Aug 2005). "Metabolism of [3H]pentosan polysulfate sodium (PPS) in healthy human volunteers". Xenobiotica 35 (8): 775–84. doi:10.1080/00498250500230586. PMID 16278190.
- ^ Parsons, C (2005). "Successful downregulation of bladder sensory nerves with combination of heparin and alkalinized lidocaine in patients with interstitial cystitis". Urology 65 (1): 45–8. doi:10.1016/j.urology.2004.08.056. PMID 15667861.
- ^ Altman, RD; Kapila, P; Dean, DD; Howell, DS (1988). "Future therapeutic trends in osteoarthritis". Scand J Rheumatol 77 (Suppll): 37–42. doi:10.3109/03009748809096934. PMID 3070732.
- ^ a b Ghosh, P (1999). "The pathobiology of osteoarthritis and the rationale for the use of pentosan polysulfate for its treatment". Semin Arthritis Rheum 28 (4): 211–67. doi:10.1016/s0049-0172(99)80021-3. PMID 10073500.
- ^ Klocking, H-P; Hauptmann, J; Richter, M (1991). "Profibrinolytic and anticoagulant properties of the pentosan polysulphate derivative bego 0391". Pharmazie 46: 543–544. PMID 1723804.
- ^ Smith, MM; Ghosh, P; Numata, Y; Bansal, M (1994). "The effects of orally administered calcium pentosan polysulfate on inflammation and cartilage degradation produced in rabbit joints by intraarticular injection of a hyaluronate-polylysine complex". Arthritis Rheum 37 (1): 125–136. doi:10.1002/art.1780370118. PMID 7510481.
- ^ Read, RA; Cullis-Hill, D; Jones, MP (1996). "Systemic use of pentosan polysulphate in the treatment of osteoarthritis". J Small Anim Pract 37 (3): 108–114. doi:10.1111/j.1748-5827.1996.tb02355.x. PMID 8683953.
- ^ Ghosh, P; Cheras, PA (2001). "Vascular mechanisms in osteoarthritis". Best Pract Res Clin Rheumatol 15 (5): 693–709. doi:10.1053/berh.2001.0188. PMID 11812016.
- ^ Innes, JF; Barr, AR; Sharif, M (2000). "Efficacy of oral calcium pentosan polysulphate for the treatment of osteoarthritis of the canine stifle joint secondary to cranial cruciate ligament deficiency". Vet Rec 146 (15): 433–437. doi:10.1136/vr.146.15.433. PMID 10811265.
- ^ Budsberg, SC; Bergh, MS; Reynolds, LR; Streppa, HK (2007). "Evaluation of pentosan polysulfate sodium in the postoperative recovery from cranial cruciate injury in dogs: a randomized, placebo-controlled clinical trial". Vet Surg 36 (3): 234–244. doi:10.1111/j.1532-950x.2007.00256.x. PMID 17461948.
- ^ Little, CB; Ghosh, P (1996). McIlwraith, CW; Trotter, GW, eds. Joint Disease in the Horse. Philadelphia: WB Saunders Company. pp. 281–292.
- ^ McIlwraith, CW; Frisbie, DD; Kawcak, CE (2012). "Evaluation of intramuscularly administered sodium pentosan polysulfate for treatment of experimentally induced osteoarthritis in horses". Am J Vet Res 73 (5): 628–633. doi:10.2460/ajvr.73.5.628. PMID 22533393.
- ^ Kramer, CM; Tsang, AS; Koenig, T; Jeffcott, LB; Dart, CM; Dart, AJ (2014). "Survey of the therapeutic approach and efficacy of pentosan polysulfate for the prevention and treatment of equine osteoarthritis in veterinary practice in Australia". Aust Vet J 92 (12): 482–487. doi:10.1111/avj.12266. PMID 25424761.
- ^ Verbruggen, G; Veys, EM (1992). "Intra-articular injection pentosanpolysulphate results in increased hyaluronan molecular weight in joint fluid". Clin Exp Rheumatol 10 (3): 249–254. PMID 1374695.
- ^ Verbruggen, G; Veys, EM (1996). "Laboratory and clinical studies on clacium pentosan polysulphate". Osteoarthritis Cartilage 4: iii-iv. doi:10.1016/s1063-4584(96)80022-7.
- ^ Rasaratnam, I; Ryan, P; Bowman, L; Smith, M; Ghosh, P (1996). "A double-blind placebo-controlled study of intra-articular pentosan polysulphate (Cartrophen) in patients with gonarthritis: laboratory and clinical findings". Osteoarthritis Cartilage 4: vi-vii. doi:10.1016/s1063-4584(96)80025-2.
- ^ Adam, N; Ghosh, P; Swain, M; Rasaratnam, I; Ryan, P (1996). "The effects of intra-articular pentosan polysulphate (Cartrophen) on synovial fluid visco-elasticity and hyaluronan molecular weight in patients with gonarthritis". Osteoarthritis Cartilage 4: viii. doi:10.1016/s1063-4584(96)80026-4.
- ^ Ghosh, P; Edelman, J; March, L; Smith, M (2005). "Effects of pentosan polysulfate in osteoarthritis of the knee: A randomized, double-blind, placebo-controlled pilot study". Curr Therap Res Clin Exp 66 (6): 552–571. doi:10.1016/j.curtheres.2005.12.012. PMID 24678076.
- ^ Kumagai, K; Shirabe, S; Miyata, N; Murata, M; Yamauchi, A; Kataoka, Y; Niwa, M (2010). "Sodium pentosan polysulfate resulted in cartilage improvement in knee osteoarthritis--an open clinical trial". BMC Clin Pharmacol 10: 7. doi:10.1186/1472-6904-10-7. PMID 20346179.
- ^ Yamasaki, Takeshi; Suzuki, Akio; Hasebe, Rie; Horiuchi, Motohiro (2014). "Comparison of the Anti-Prion Mechanism of Four Different Anti-Prion Compounds, Anti-PrP Monoclonal Antibody 44B1, Pentosan Polysulfate, Chlorpromazine, and U18666A, in Prion-Infected Mouse Neuroblastoma Cells". PLOS ONE 9 (9): e106516. doi:10.1371/journal.pone.0106516. PMID 25181483.
- ^ Kamatari, Yuji O; Hayano, Yosake; Yamaguchi, Kei-ichi; Hosokawa-Muto, Junji; Kuwata, Kazuo (2012). "Characterizing antiprion compounds based on their binding properties to prion proteins: Implications as medical chaperones". Protein Sci 22: 22–34. doi:10.1002/pro.2180. PMID 23081827.
- ^ Whittle, IR; Knight, RS; Will, RG (2006). "Unsuccessful intraventricular pentosan polysulphate treatment of variant Creutzfeldt-Jakob disease". Acta Neurochir (Wien) 148: 677–679. doi:10.1007/s00701-006-0772-y. PMID 16598408.
- ^ BBC NEWS | Health | Research will now assess CJD drug
- ^ a b Pubmed Health (2012). "Pentosan Polysulfate". U.S. National Library of Medicine. Retrieved 2 October 2012.
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