Last Updated: September 28 2022

Serrapeptase is an enzyme derived from silkworms. It has anti-inflammatory effects and can help prevent blood clots, but these effects are somewhat unreliable.

Serrapeptase is most often used for.

Don't miss out on the latest research


Sources and Structure



Serrapeptase is a proteolytic enzyme touted for anti-inflammatory, anti-edemic, and analgesic properties and appears to be active following oral ingestion of an enteric coated capsule.[1] Brand names for serrapeptase include Danzen, Serodase, Nemesulide, and Antiflazym.

Serrapeptase is produced from Serratia bacteria, found in the intestines of the silkworm (Bombyx mori) which sometimes leads to serrapeptase being referred to as 'silkworm enzymes'. Of the various species of serratia bacteria that can produce protease enzymes (indica, marcescens, plymuthica, and piscatorum). Serratia marcescens has a particular strain known as E15 (ATCC 13880[2]) that has up to a threefold greater yeild[3][1] and although marcescens in general is preferred for production of serrapeptase[4][5][6] the E15 strain is favored.

Serrapeptase is not the only enzyme found from these bacteria, but is the major enzyme produced (three other larger but less common enzymes are also produced).[7]



The serrapeptase enzyme has a molecular weight of 45,000-60,000Da (50.6kDa reported elsewhere[8]) and is comprised of 470 amino acids in length; it is classified as a metalloprotease due to containing a zinc molecule which helps catalyze its enzymatic activity.[7][9] Although it shows maximal activity at 40°C and a pH of 9.0, it is fully inactivated at 55°C for 15min[9][1] and possesses an isoelectric point of 5.3.[7]

It's substrate specificity appears to be somewhat similar to that of thermolysin (produced from bacillus thermoproteolyticus),[9] and the amino acid sequence is free of sulfur containing amino acids (cysteine and methionine).[7]

Appears to be a rather large metalloprotease enzyme, which can be inactivated (rendered useless) by excess heat





Due to the supplement in question being an enzyme and destroyed in the acidic environment of the stomach,[7] enteric coated capsules (resistant to acidity, and thus degrade in the intestines rather than the stomach[10]) are used. Aquasomes (a carrier comprised of a nanocrystalline core coated with polyhydroxy oligomers[11]) follow a similar idea, where it is stable for 2-6 hours in acidic medium (pH 1.2) and has a linear release rate in alkaline medium (pH 7.4).[12]

Serrapeptase is destroyed in the acidic environment of the stomach, and as such would require enteric encapsulation in order to retain the bioactivity

Despite being a large protein structure, serrapeptase has been found to be absorbed in the rat intestine following oral administration,[13] although the large structure and possible degradation in the intestines has been cited to possible reduce the bioavailability of serrapeptase (enzymes are readily degraded by drastic changes in pH and large protein structures may not be absorbed well[14]).

Serrapeptase alone appears to have low permeability in a Caco-2 model of intestinal permeability (–7.72+/- 0.51cm/s[15]) which appears to slightly improved with liposomal delivery systems (phosphatidylcholine up to -7.47+/-0.36cm/s and 1,2-dimyristoyl-sn-glycero-3-phosphoethanolamine up to -6.5+/-0.35cm/s).[15] It was noted that this may underestimate the absorption of serrapeptase a bit, as Caco-2 cells have tighter gap junctions than do in vivo conditions (and thus less paracellular transport).[15]

The enhanced absorption of serrapeptase with liposomes is thought to due to liposomes increasing paracellular (between cells) transport of molecules[16][17] and serrapeptase being too large for transport-mediated absorption (and thus likely mediated by paracellular transport).

Serrapeptase, surprisingly, is absorbed through the intestinal wall similar to bromelain and appears to retain its enzymatic activity. It appears to be absorbed paracellularly (between cells), but does not appear to be well absorbed although it is enhanced by liposomes

Serrapeptase has been thought to be used topically, although isopropyl myristate (IPM) or dimethyl sulfoxide (DMSO) are required to enhance skin absorption (due to serrapeptase being a large enzyme structure) and were required at higher than acceptable concentrations according to the authors.[18] In a rat anti-edema test, a topical gel (Monegyl 0100 at 10%, PEG 400 at 40%, Propylene glycol at 10%, 1% serrapeptase, and PEG 4000 added until mixture congeals) was comparable in efficacy to a diclofenac gel suggesting some bioactivity.[18]

Other delivery methods that have been reported are a glyceryl monooleate based system.[19]

There is limited evidence that serrapeptase can be bioactive topically, which needs to be re-evaluated and mechanisms investigated more (as it is quite illogical for a large protein structure to be absorbed via the skin)



It has been detected in serum following an oral dose of 100mg/kg (rats) to 0.87+/-0.41ng/mL, and in lymph it had higher concentrations of 43+/-42ng/mL at a Tmax of 15-30 minutes.[13] A minimum dose of 30mg/kg was required to find any detectable concentration in plasma, yet only 1mg/kg for a level in lymph tissue.[13]

In rats it appears to travel through the blood bound to plasma protease inhibitor alpha-1 macroglobulin (α1M) in a 1:1 ratio; this has been noted to reduce the enzymatic activity to about 20% of its inhernet value, but a value still appears to be present.[20]



Serrapeptase has been found to be distributed to sites of inflammation in the rat (careegnaan induced) to a concentration higher than serum.[13]





Pain has been noted to be reduced on days 1-5 after jaw surgery with 15mg serrapeptase relative to placebo (study confounded with 1000mg paracetamol in both groups) but no significant difference on day 7, with a 3 point reduction on day 1 (VAS scale; a rating from 0-10) and a 1 point difference afterwards.[21]

A study in breast pain (engorgement and swelling) noted that 30mg of serrapeptase for 3 days was able to increase the amount of response (persons who reported pain reduction) from 60% to 85.7% and increase reported 'marked improvements' in pain from 2.9% in placebo to 22.9%.[22]


Inflammation and Immunology



It is claimed that the enzymatic activity of serrapeptase (appears to be somewhat preserved following oral ingestion) is able to hydrolyze bradykinin, histamine and serotonin which are responsible for edemic processes.[23][24]


Small Joint Inflammation

10mg of serrapeptase thrice a day the day prior to and of surgery (maxillary sinus antrotomy) as well as for 5 subsequent days (7 days in total), relative to placebo, was able to significantly reduce jaw swelling at all measured time points.[25]

In patients undergoing removal of third molars given paracetamol (1000mg) paired with serrapeptase (15mg daily, 5mg taken every 8 hours for 7 days) or placebo, there was a significantly reduction in cheek swelling on all measured days except immediately after surgery while pain followed the opposite trend (significantly more effective than placebo days 1-5 after surgery, but not day 7); interincisal difference was not affected.[21] Other studies on third molar surgeries noted that either serrapeptase is ineffective in reducing inflammation[26] or the standard 30mg dose is effective, but to a lesser degree than 3mg dexamethasone (1mg thrice daily).[27]

The research looking at jaw inflammation appears to support the usage of serrapeptase, but aside from the studies being limited it appears to be less effective than the reference drug (dexamethasone)

One study in carpal tunnel syndrome given an initial course of nimesulide and then followed up with 10mg serrapeptase twice daily (20mg daily) for 6 weeks noted a 65% response rate for 'significant improvement' but did not have a placebo group for comparison.[28]

The evidence to support a role in carpal tunnel syndrome is, methodologically speaking, quite weak


Other Interventions

In rats, the anti-inflammatory effects of serrapeptase at 10-20mg/kg was compaed against 0.5mg/kg diclofenac (for both an acute inflammation study over 8 hours and a chronic inflammation study over 9 days) noted that all groups were comparable in reducing paw edema acutely (43.18-54.55% suppression of paw edema) but there appeared to be dose-dependence for chronic inflammation where 10mg/kg serrapeptase underperformed diclofenac (40% inhibition of paw edema relative to 72%) while 20mg/kg was comparable (68% relative to 72%).[24]

Anti-inflammatory effects appear to exist in rats following oral ingestion

A meta-analysis[1] of 14 trials noted that the six positive trials included (five can be found online[29][22][28][30][25]) were fairly low quality, with three trials not disclosed the given dose and one not compared to any control or placebo group; the final two studies that were positive were in treating jaw swelling after maxillary sinus antrotomy surgery[25] and for reducing breast engorgement ('marked improvement' was 22.9% with serrapeptase, 2.9% with placebo);[22] both studies used 30mg daily in three doses of 10mg for 7-14 days.

The studies that support the efficacy of serrapeptase appear to be low in quality


Biofilms and Mucus

In staphylococci bacteria (epidermidis and aureus populating human skin and mucus membranes) are bacteria that can produce protein-dependent biofilms[31][32] and protease enzymes are a class of molecules which are sometimes used to disperase these biofilms.[33] At 50U/mL (2.5mcg/mL), serrapeptase was able to inhibit biofilm production of all tested strains (aureus strains ATCC 6538P, 25923, 35984, and 12598 as well as epidermis strains XX-17 and O-47).[34][35] Efficacy has also been noted against 5 strains of Pseudomonas aeruginosa[8] and Listeria monocytogenes.[36]

In a comparative analysis, serrapeptase was more potent than other tested proteases (Clostridiopeptidase A, fibrinolysin, and streptokinase).[8]

For bacteria that create protein-dependent biofilms, it appears that serrapeptase may have an inhibitory effect on biofilm production

Biofilms are used by bacteria to, aside from adherence to cells, to prevent infiltration of the bacteria cell from antibacterial agents[37][38] and in vitro serrapeptase (100U/mL; 5mcg/mL) has been found to augment the anti-bacterial properties of ofloxacin by approximately halving the minimum inhibitory concentration.[8]

In vitro, serrapeptase has been found to augment antibacterials which is thought to be from reducing biofilm production (which then enhances the ability of the antibacterial agent to target the bacteria since it is removing the bacterial defenses). These have not yet been noted in a living model

Serrapeptase is known as a mucus liquifying agent[39] and 30mg of serrapeptase daily for 4 weeks in persons with chronic airway diseases has been noted to significantly decrease sputum weight and neutrophil count as well as its viscosity and elasticity;[40] a significant decrease in the frequency of coughing and expectoration was also noted.[40]

Elsewhere, serrapeptase has been noted to reduce dynamic viscosity of nasal secretion with affecting the elastic modulus[41] and this effect (a reduction in viscosity but not elasticity) has been noted elsewhere following oral ingestion of 30mg serrapeptase daily for 4 weeks.[42] Other studies, however, either note a decrease in both viscosity and elasticity (lung sputum)[40] or a decrease in viscoelasticity.[43] While the decrease in viscosity appears to be reliable, the elasticity is not as much.

Appears to alter mucus secretions of the body. Although there is not an ample amount of evidence for this, it may be of use to persons with chronically stuffed noses (sinusitis) and for lung symptoms of cystic fibrosis (currently untested)

The biofilm reducing properties of serrapeptase have also been noted to be of use in rats given a surgery with risk for infection afterwards (by biofilm producing bacteria), where the occurrence rates of bacterial growth on the surgical site of 63.2% (control) was reduced with antibiotic treatment (37.5%) and synergistically reduced with the addition of serrapeptase to antibiotics (5.6%).[44]


Nutrient-Nutrient Interactions



Serrapeptase appears to be synergistic with antibiotic drugs and molecules. Serrapeptase has the ability to reduce the biofilms produced by select bacteria and these biofilms can impair the ability of antibiotics to destroy a bacteria.[37][38]

In vitro, serrapeptase (100U/mL; 5mcg/mL) has been found to augment the anti-bacterial properties of ofloxacin by approximately halving the minimum inhibitory concentration[8] and in a rat model of surgery where the occurrence of bacterial infection in control (63.2%) was reduced to 37.5% with antibiotics but down to 5.6% with the combination treatment of antibiotics and serrapeptase.[44]

Elsewhere in rabbits, the plasma concentrations of Cefotiam appear to be increased following coingestion of serrapeptase, while only increasing tissue concentrations in the rabbit model of pneumonitis (no effect in pleuritis)[45] and has been noted to increae gingival concentrations of four antibiotic drugs (Ciclacillin, ampicillin, cephalexin, and minocycline) in rats given 20mg/kg serrapeptase.[46]

Appears to augment antibiotic efficacy by reducing the inhibitory effects of bacterial biofilms



One study assessing the interactions of injections of proteolytic enzymes (Serrapeptase, chymotrypsin, or trypsin) and aspirin noted that all enzymes were synergistic with aspirin in acute and subacute inflammatory tests in rats;[47] this study also noted that 90-270µg/kg serrapeptase was equivalent to 200mg/kg (oral ingestion) and was equivalent to trypsin (288-576µg/kg) and chymotrypsin (18-36mg/kg) in potency.[47]


Safety and Toxicity



A systemic review on serrapeptase[1] has noted that there are limited adverse drug reactions reported, but they tend to be related to skin conditions (such as erythema or dermatosis[48]) and both muscle and joint pain; there appear to be some reported coagulation problems.[1]

Commonly said to be safe (although there really isn't any robust toxicological data on this claim) and has been linked to sporadic side-effects related to joints and the skin. Occurrence rates are not known, but they seem rare

1.^Bhagat S, Agarwal M, Roy VSerratiopeptidase: a systematic review of the existing evidenceInt J Surg.(2013)
2.^Badhe RV, Nanda RK, Kulkarni MB, Bhujbal MN, Patil PS, Badhe SRMedia optimization studies for Serratiopeptidase production from Serratia marcescens ATCC 13880Hindustan Antibiot Bull.(2009)
6.^Bromke BJ, Hammel JMRegulation of extracellular protease formation by Serratia marcescensCan J Microbiol.(1979 Jan)
7.^Matsumoto K, Maeda H, Takata K, Kamata R, Okamura RPurification and characterization of four proteases from a clinical isolate of Serratia marcescens kums 3958J Bacteriol.(1984 Jan)
8.^Selan L, Berlutti F, Passariello C, Comodi-Ballanti MR, Thaller MCProteolytic enzymes: a new treatment strategy for prosthetic infectionsAntimicrob Agents Chemother.(1993 Dec)
11.^Umashankar MS, Sachdeva RK, Gulati MAquasomes: a promising carrier for peptides and protein deliveryNanomedicine.(2010 Jun)
13.^Moriya N, Nakata M, Nakamura M, Takaoka M, Iwasa S, Kato K, Kakinuma AIntestinal absorption of serrapeptase (TSP) in ratsBiotechnol Appl Biochem.(1994 Aug)
14.^Woodley JFEnzymatic barriers for GI peptide and protein deliveryCrit Rev Ther Drug Carrier Syst.(1994)
17.^Obata K, Sugano K, Saitoh R, Higashida A, Nabuchi Y, Machida M, Aso YPrediction of oral drug absorption in humans by theoretical passive absorption modelInt J Pharm.(2005 Apr 11)
20.^Kakinuma A, Moriya N, Kawahara K, Sugino HRepression of fibrinolysis in scalded rats by administration of Serratia proteaseBiochem Pharmacol.(1982 Sep 15)
24.^Jadav SP, Patel NH, Shah TG, Gajera MV, Trivedi HR, Shah BKComparison of anti-inflammatory activity of serratiopeptidase and diclofenac in albino ratsJ Pharmacol Pharmacother.(2010 Jul)
25.^Tachibana M, Mizukoshi O, Harada Y, Kawamoto K, Nakai YA multi-centre, double-blind study of serrapeptase versus placebo in post-antrotomy buccal swellingPharmatherapeutica.(1984)
28.^Panagariya A, Sharma AKA preliminary trial of serratiopeptidase in patients with carpal tunnel syndromeJ Assoc Physicians India.(1999 Dec)
32.^Christner M, Franke GC, Schommer NN, Wendt U, Wegert K, Pehle P, Kroll G, Schulze C, Buck F, Mack D, Aepfelbacher M, Rohde HThe giant extracellular matrix-binding protein of Staphylococcus epidermidis mediates biofilm accumulation and attachment to fibronectinMol Microbiol.(2010 Jan)
34.^Artini M, Papa R, Scoarughi GL, Galano E, Barbato G, Pucci P, Selan LComparison of the action of different proteases on virulence properties related to the staphylococcal surfaceJ Appl Microbiol.(2013 Jan)
35.^Artini M, Scoarughi GL, Papa R, Cellini A, Carpentieri A, Pucci P, Amoresano A, Gazzola S, Cocconcelli PS, Selan LA new anti-infective strategy to reduce adhesion-mediated virulence in Staphylococcus aureus affecting surface proteinsInt J Immunopathol Pharmacol.(2011 Jul-Sep)
36.^Longhi C, Scoarughi GL, Poggiali F, Cellini A, Carpentieri A, Seganti L, Pucci P, Amoresano A, Cocconcelli PS, Artini M, Costerton JW, Selan LProtease treatment affects both invasion ability and biofilm formation in Listeria monocytogenesMicrob Pathog.(2008 Jul)
38.^Costerton JW, Cheng KJ, Geesey GG, Ladd TI, Nickel JC, Dasgupta M, Marrie TJBacterial biofilms in nature and diseaseAnnu Rev Microbiol.(1987)
39.^Lee HS, Majima Y, Sakakura Y, Kim BWA technique for quantitative cytology of nasal secretionsEur Arch Otorhinolaryngol.(1991)
40.^Nakamura S, Hashimoto Y, Mikami M, Yamanaka E, Soma T, Hino M, Azuma A, Kudoh SEffect of the proteolytic enzyme serrapeptase in patients with chronic airway diseaseRespirology.(2003 Sep)
41.^Majima Y, Hirata K, Takeuchi K, Hattori M, Sakakura YEffects of orally administered drugs on dynamic viscoelasticity of human nasal mucusAm Rev Respir Dis.(1990 Jan)
42.^Majima Y, Inagaki M, Hirata K, Takeuchi K, Morishita A, Sakakura YThe effect of an orally administered proteolytic enzyme on the elasticity and viscosity of nasal mucusArch Otorhinolaryngol.(1988)
43.^Shimura S, Okubo T, Maeda S, Aoki T, Tomioka M, Shindo Y, Takishima T, Umeya KEffect of expectorants on relaxation behavior of sputum viscoelasticity in vivoBiorheology.(1983)
44.^Mecikoglu M, Saygi B, Yildirim Y, Karadag-Saygi E, Ramadan SS, Esemenli TThe effect of proteolytic enzyme serratiopeptidase in the treatment of experimental implant-related infectionJ Bone Joint Surg Am.(2006 Jun)
47.^Viswanatha Swamy AH, Patil PAEffect of some clinically used proteolytic enzymes on inflammation in ratsIndian J Pharm Sci.(2008 Jan)
48.^Shimizu H, Ueda M, Takai T, Bito T, Ichihashi M, Muramatsu T, Shirai TA case of serratiopeptidase-induced subepidermal bullous dermatosisBr J Dermatol.(1999 Dec)