Cantharidin
Beetles
Okadaic Acid
Phosphoprotein Phosphatases
Cobra Cardiotoxin Proteins
The protein phosphatase inhibitor cantharidin induces head and foot formation in buds of Cassiopea andromeda (Rhizostomae, Scyphozoa). (1/89)
The polyps of Cassiopea andromeda produce spindle shaped, freely swimming buds which do not develop a head (a mouth opening surrounded by tentacles) and a foot (a sticky plate at the opposite end) until settlement to a suited substrate. The buds, therewith, look very similar to the planula larvae produced in sexual reproduction. With respect to both, buds and planulae, several peptides and the phorbolester TPA have been found to induce the transformation into a polyp. Here it is shown that cantharidin, a serine/threonine protein phosphatase inhibitor, induces head and foot formation in buds very efficiently in a 30 min treatment, the shortest yet known efficient treatment. Some resultant polyps show malformations which indicate that a bud is ordinary polyp tissue in which preparatory steps of head and foot formation mutually block each other from proceeding. Various compounds related to the transfer of methyl groups have been shown to affect head and foot formation in larvae of the hydrozoon Hydractinia echinata. These compounds including methionine, homocysteine, trigonelline, nicotinic acid and cycloleucine are shown to also interfere with the initiation of the processes which finally lead to head and foot formation in buds of Cassiopea andromeda. (+info)The protein phosphatase inhibitor cantharidin alters vascular endothelial cell permeability. (2/89)
In this study, we characterized the effects of the protein phosphatases type 1 (PP 1) and type 2A (PP 2A) inhibitor cantharidin in endothelial cells. We identified catalytic subunits of PP 1alpha, PP 2Aalpha, and PP 2Abeta immunologically in bovine aortic endothelial cells. Moreover, we detected mRNAs coding for catalytic subunits of PP 1alpha, PP 1beta, and PP 2Aalpha by hybridization with specific DNA probes in total RNA from these cells. Okadaic acid and cantharidin inhibited the activities of catalytic subunits of PP 1 (okadaic acid, 0.01-1 microM; cantharidin, 1-100 microM) and PP 2A (okadaic acid, 0.1 nM to 1 microM; cantharidin, 0.1-100 microM) separated by column chromatography in a concentration-dependent manner. Moreover, cantharidin (1 microM to 1 mM) increased the phosphorylation state of endothelial proteins including the regulatory light chains of myosin without affecting cytosolic calcium concentrations. Cantharidin (5-100 microM) increased the permeability of cultured endothelial cells in a time- and concentration-dependent manner. We suggest that inhibition of PP 1 and PP 2A activities by cantharidin increases endothelial permeability by enhancing the phosphorylation state of endothelial regulatory proteins. Thus, cantharidin might be a useful tool to study the function of protein phosphatases in endothelial barrier function. (+info)Penetration of moxifloxacin into peripheral compartments in humans. (3/89)
To characterize the penetration of moxifloxacin (BAY 12-8039) into peripheral target sites, the present study aimed at measuring unbound moxifloxacin concentrations in the interstitial space fluid by means of microdialysis, an innovative clinical sampling technique. In addition, moxifloxacin concentrations were measured in cantharides-induced skin blisters, saliva, and capillary plasma and compared to total- and free-drug concentrations in venous plasma. For this purpose, 12 healthy volunteers received moxifloxacin in an open randomized crossover fashion either as a single oral dose of 400 mg or as a single intravenous infusion of 400 mg over 60 min. An almost-complete equilibration of the free unbound plasma fraction of moxifloxacin with the interstitial space fluid was observed, with mean area under the concentration-time curve (AUC)(interstitial fluid)/AUC(total-plasma) ratios ranging from 0.38 to 0.55 and mean AUC(interstitial fluid)/AUC(free-plasma) ratios ranging from 0.81 to 0.86. The skin blister concentration/plasma concentration ratio reached values above 1.5 after 24 h, indicating a preferential penetration of moxifloxacin into inflamed lesions. The moxifloxacin concentrations in saliva and capillary blood were similar to the corresponding levels in plasma. Our data show that moxifloxacin concentrations attained in the interstitial space fluid in humans and in skin blister fluid following single doses of 400 mg exceed the values for the MIC at which 90% of isolates are inhibited for most clinically relevant bacterial strains, notably including penicillin-resistant Streptococcus pneumoniae. These findings support the use of moxifloxacin for the treatment of soft tissue and respiratory tract infections in humans. (+info)A study to determine the pharmacokinetics and inflammatory fluid penetration of gatifloxacin following a single oral dose. (4/89)
A single 400 mg oral dose of gatifloxacin was given to each of nine healthy male volunteers and the concentrations of the drug in plasma, cantharidine-induced inflammatory fluid and urine were measured over the following 24 h. The mean peak concentration in plasma of 4. 1 mg/L was attained at a mean time of 1.8 h post dose. The mean peak concentration in inflammatory fluid was 3.6 mg/L and was attained at a mean time of 4.2 h post dose. The mean plasma elimination half-life of gatifloxacin was 6.8 h and that in inflammatory fluid was 7.2 h. The mean penetration into the inflammatory fluid was 117%. Recovery of drug from urine during the first 24 h post dose was 65% of that administered. Our data suggest that gatifloxacin dosed at 400 mg od should be adequate to treat systemic infections caused by most bacterial species. (+info)Phosphatase inhibitor cantharidin blocks adenosine A(1) receptor anti-adrenergic effect in rat cardiac myocytes. (5/89)
Experiments were performed to examine whether the protein phosphatase inhibitor cantharidin blocks the anti-adrenergic effect of adenosine A(1) receptor stimulation. In electrically stimulated adult rat ventricular myocytes loaded with the intracellular calcium concentration ([Ca(2+)](i)) indicator fluo-3, isoproterenol (10 nM) increased systolic [Ca(2+)](i) by 46%, increased twitch amplitude by 56%, and increased total cellular cAMP content by 140%. The adenosine A(1) receptor agonist 2-chloro-N(6)-cyclopentlyadenosine (CCPA) reduced isoproterenol-stimulated [Ca(2+)](i) and contractility by 87 and 80%, respectively, but reduced cAMP content by only 18%. Cantharidin had no effects on myocyte [Ca(2+)](i), contractility, or cAMP in the absence or presence of isoproterenol but blocked the effects of CCPA on [Ca(2+)](i) and contractility by approximately 44%. Cantharidin had no effect on CCPA attenuation of isoproterenol-induced increases in cAMP. Pretreatment with CCPA also reduced the increase in contractile parameters produced by the direct cAMP-dependent protein kinase A (PKA) activator 8-bromocAMP. These results suggest that activation of protein phosphatases mediate, in part, the anti-adrenergic effect of adenosine A(1) receptor activation in ventricular myocardium. (+info)Hamster pancreatic beta cell lines with altered sensitivity towards apoptotic signalling by phosphatase inhibitors. (6/89)
Specific inhibitors of serine/threonine phosphatases like okadaic acid can induce apoptotic cell death in the pancreatic beta cell line HIT. Cultivation in stepwise increased concentrations of okadaic acid enabled the isolation of HIT100R cells which proliferate at 100 nM okadaic acid (8 - 10 times the initially lethal concentration). These two cell lines were used to characterize the events triggered by okadaic acid that led to apoptosis. Biochemical markers, e.g. cytochrome c release from mitochondria and increase of caspase-3-like activity, revealed that induction of apoptosis by 100 nM okadaic acid in parental HIT cells started with the release of cytochrome c. In HIT100R cells 500 nM okadaic acid were necessary to induce alterations comparable to those observed with 100 nM okadaic acid in non-resistant HIT cells. In contrast to okadaic acid, the potency of the structurally different phosphatase inhibitor cantharidic acid to induce cytochrome c release, increase of caspase-3-like activity and DNA fragmentation was comparable in HIT and HIT100R cells. Thus, no cross-resistance between these phosphatase inhibitors seemed to exist. Phosphatase activity in extracts from HIT and HIT100R cells did not differ in its total amount or in its sensitivity for okadaic acid. Since higher concentrations of okadaic acid were needed to induce apoptosis in HIT100R cells, a compromised intracellular accumulation of the toxin appeared likely. Functional and structural analysis revealed that this was achieved by the development of the multidrug resistance phenotype in HIT100R cells. The underlying mechanism appeared to be the enhanced expression of the pgp1 but not the pgp2 gene. (+info)Protein phosphatase inhibitors arrest cell cycle and reduce branching morphogenesis in fetal rat lung cultures. (7/89)
Protein phosphatase 2A (PP2A) is a key signal transduction intermediate in the regulation of cellular proliferation and differentiation in vitro. However, the role of PP2A in the context of a developing organ is unknown. To explore the role of PP2A in the regulation of lung development, we studied the effect of PP2A inhibition on new airway branching, induction of apoptosis, DNA synthesis, and expression of epithelial marker genes in whole organ explant cultures of embryonic (E14) rat lung. Microdissected lung primordia were cultured in medium containing one of either two PP2A inhibitors, okadaic acid (OA, 0-9 nM) or cantharidin (Can, 0-3,600 nM), or with the PP2B inhibitor deltamethrin (Del, 0-10 microM) as a control for a PP2A-specific effect for 48 h. PP2A inhibition with OA and Can significantly inhibited airway branching and overall lung growth. PP2B inhibition with Del did not affect lung growth or new airway development. Histologically, both PP2A- and PP2B-inhibited explants were similar to controls. Increased apoptosis was not the mechanism of decreased lung growth and new airway branching inasmuch as OA-treated explant sections subjected to the terminal deoxynucleotidyltransferase dUTP nick end labeling reaction demonstrated a decrease in apoptosis. However, PP2A inhibition with OA increased DNA content and 5-bromo-2'-deoxyuridine uptake that correlated with a G(2)/M cell cycle arrest. PP2A inhibition also resulted in altered differentiation of the respiratory epithelium as evidenced by decreased mRNA levels of the early epithelial marker surfactant protein C. These findings suggest that inhibition of protein phosphatases with OA and Can halted mesenchymal cell cycle progression and reduced branching morphogenesis in fetal rat lung explant culture. (+info)Cantharidin enhances norepinephrine-induced vasoconstriction in an endothelium-dependent fashion. (8/89)
In this study we characterized the effects of the protein phosphatase (PP) type 1 and type 2A inhibitor cantharidin (Cant) and its structural analogs cantharidic acid and endothall on PP activity, force of contraction, and myosin light chain phosphorylation in rat aorta. All compounds inhibited PP activity in homogenates of rat aorta with a rank order of potency of Cant = cantharidic acid > endothall. However, only Cant increased force of contraction and myosin light chain phosphorylation in intact isolated rat aortic rings. Based on these findings, we investigated the effects of Cant on alpha-adrenoceptor-mediated vasoconstriction. Cant (1 and 3 microM) enhanced norepinephrine-induced contraction in endothelium-intact rat aorta. In contrast, Cant did not affect norepinephrine-induced contraction in endothelium-denuded rat aorta. We suggest that inhibition of PP1 and/or PP2A activities by Cant enhances vascular contractility in endothelium-intact rat aorta by increasing the phosphorylation state of endothelial regulatory proteins. (+info)Cantharidin is a toxic alkaloid found in certain species of blister beetles, such as the Spanish fly. It is known for its powerful irritant and vesicant properties, causing severe blistering and inflammation of the skin and mucous membranes upon contact. In the medical field, cantharidin is sometimes used as a topical treatment for warts and other skin growths. However, it is highly toxic and can cause serious side effects, including nausea, vomiting, diarrhea, abdominal pain, and even death in high doses. Therefore, its use is generally restricted to medical professionals and requires careful monitoring and dosage control.
In the medical field, beetles are not typically studied or used for medical purposes. Beetles are a type of insect that belong to the order Coleoptera, which is the largest order of insects. They are known for their hard exoskeletons, which protect their internal organs. However, some species of beetles are used in medical research for their potential as sources of new drugs or as models for studying human diseases. For example, the beetle species Tribolium castaneum has been used in research on aging and cancer, while the beetle species Tenebrio molitor is used in the production of silkworms and has been studied for its potential as a source of therapeutic compounds. In general, beetles are not commonly associated with medical treatments or interventions, but their unique biological characteristics and potential applications in research make them an interesting subject of study for scientists.
Okadaic acid is a potent marine toxin produced by certain species of dinoflagellates, which are microscopic algae found in marine environments. It is a member of a group of toxins called polyether lipids, which are also known as diarrhetic shellfish poisoning (DSP) toxins. In the medical field, okadaic acid is primarily associated with seafood poisoning, which can occur when contaminated shellfish are consumed. The symptoms of okadaic acid poisoning can include nausea, vomiting, diarrhea, abdominal pain, and fever. In severe cases, it can lead to liver damage, kidney failure, and even death. Okadaic acid is also being studied for its potential therapeutic uses. Some research has suggested that it may have anti-cancer properties and may be useful in the treatment of certain types of cancer. However, more research is needed to confirm these findings and to determine the safety and efficacy of okadaic acid as a cancer treatment.
Phosphoprotein phosphatases are enzymes that remove phosphate groups from phosphoproteins, which are proteins that have been modified by the addition of a phosphate group. These enzymes play a crucial role in regulating cellular signaling pathways by modulating the activity of phosphoproteins. There are several types of phosphoprotein phosphatases, including protein tyrosine phosphatases (PTPs), protein serine/threonine phosphatases (S/T phosphatases), and phosphatases that can dephosphorylate both tyrosine and serine/threonine residues. Phosphoprotein phosphatases are involved in a wide range of cellular processes, including cell growth and division, metabolism, and immune response. Dysregulation of phosphoprotein phosphatase activity has been implicated in various diseases, including cancer, diabetes, and neurodegenerative disorders.
In the medical field, copulation refers to the sexual act of penetration between a male and female reproductive organ, typically involving intercourse. It is a common form of sexual activity and is often associated with reproduction, although it can also occur for pleasure or other reasons. Copulation typically involves the penis penetrating the vagina, although other forms of sexual activity, such as anal or oral sex, can also occur. It is important to note that copulation can carry risks, including the transmission of sexually transmitted infections (STIs) and unwanted pregnancies, and it is important to practice safe sex to minimize these risks.
Cobra cardiotoxin proteins are a type of venom found in certain species of cobras, such as the Indian cobra and the king cobra. These proteins are known to be potent toxins that can cause damage to the heart muscle and lead to cardiac arrest. When a cobra injects its venom into a victim, the cardiotoxin proteins can interfere with the normal functioning of the heart's electrical system, leading to abnormal heart rhythms and potentially causing the heart to stop beating altogether. This can be a life-threatening condition, and prompt medical attention is necessary to prevent serious complications. In addition to their effects on the heart, cobra cardiotoxin proteins have also been shown to have other biological effects, such as causing inflammation and disrupting the normal functioning of nerve cells. As a result, these toxins have been the subject of extensive research in the fields of pharmacology and toxicology, with the goal of developing new treatments for a variety of medical conditions.
Cantharidin
It's True! It's True!
Blister beetle
Hycleus pustulatus
Hycleus phaleratus
Diels-Alder reaction
Ruth G. Capen
List of traditional Chinese medicines
Spanish fly
Endothall
Economic entomology
Cantharidic acid
Insect pheromones
Korean bug
Tegrodera aloga
Epicauta vittata
Molluscum contagiosum
Wladimir Wertelecki
Ceroctis capensis
N-Bromosuccinimide
Meloe
Sexual selection in birds
Zoopharmacognosy
Heroic medicine
Alfred Chobaut
Spur-winged goose
Equine exertional rhabdomyolysis
Juvenile hormone acid O-methyltransferase
Neopyrochroa flabellata
Epicauta
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Molluscum contagiosum3
- It is not known exactly how cantharidin works to treat molluscum contagiosum. (medlineplus.gov)
- Vakharia PP, Chopra R, Silverberg NB, Silverberg J. Efficacy and safety of topical cantharidin treatment for molluscum contagiosum and warts: a systematic review [published online August 10, 2018]. (dermatologyadvisor.com)
- Introduction however, mechanical removal (via curettage, cryotherapy, or laser treatment) and various topical therapies (including tretinoin, Molluscum contagiosum (MC) is a superficial infection of the cantharidin, Imiquimod, cidofovir) are sometimes utilized to dermis caused by a virus in the family Poxviridae. (cdc.gov)
Chemical called cantharidin2
- This fluid contains a chemical called cantharidin, which can cause blisters on the skin. (whatsthatbug.com)
- They contain a chemical called cantharidin that is extremely toxic to horses. (vin.com)
Wart2
- Wart removal is performed by applying medications like salicylic acid or cantharidin onto the wart. (whatclinic.com)
- The man says that the doctor he saw began to treat the wart with cantharidin, an agent made from a beetle that causes the area it comes in contact with to blister. (rightwingnews.com)
Topical21
- Topical cantharidin should only be applied to skin and should not be applied to the mouth, nose, eyes, or genital areas. (medlineplus.gov)
- Do not touch the treated areas of your skin or allow topical cantharidin to come in contact with your eyes or mouth for 24 hours after the medication is applied or until after it has been washed off the skin. (medlineplus.gov)
- Topical cantharidin may cause severe eye injury if it comes in contact with your or your child's eyes, including scarring and ulcers in your eyes and permanent loss of vision. (medlineplus.gov)
- If topical cantharidin comes in contact with your or your child's eyes, flush the eye for at least 15 minutes and get emergency medical treatment. (medlineplus.gov)
- Topical cantharidin may cause blistering or severe pain at the application site. (medlineplus.gov)
- If you have a severe reaction at the application site sooner than 24 hours after topical cantharidin was applied, wash the medication off of your skin with soap and water and call your doctor. (medlineplus.gov)
- Topical cantharidin is flammable, even after it has dried on the skin. (medlineplus.gov)
- Talk to you doctor if you have any questions about your treatment with topical cantharidin. (medlineplus.gov)
- tell your doctor and pharmacist if you are allergic to cantharidin, any other medications, or any of the ingredients in cantharidin topical solution. (medlineplus.gov)
- If you become pregnant while receiving topical cantharidin, call your doctor. (medlineplus.gov)
- If you are breast-feeding, your doctor will avoid applying topical cantharidin to areas of your skin that your baby could come in contact with. (medlineplus.gov)
- Topical cantharidin is flammable. (medlineplus.gov)
- Topical cantharidin may cause side effects. (medlineplus.gov)
- Topical cantharidin showed high efficacy and safety for the treatment of warts, especially when used with podophyllotoxin and salicylic acid, according to research published in the American Journal of Clinical Dermatology . (dermatologyadvisor.com)
- Study investigators performed a systematic review of the available literature and research in regard to the treatment of MC or warts with topical cantharidin. (dermatologyadvisor.com)
- Treatment for warts demonstrated significant clearance and maintenance of clearance with use of topical cantharidin monotherapy. (dermatologyadvisor.com)
- Investigators conclude that topical treatment for warts with cantharidin is effective, safe, and well tolerated among patients. (dermatologyadvisor.com)
- Topical treatment of plantar warts with compounds that include cantharidin and podophyllotoxin and salicylic acid consistently demonstrated 100% clearance rates across studies. (dermatologyadvisor.com)
- Topical treatment of MC with cantharidin as a monotherapy demonstrated variable efficacy but was well tolerated and had good treatment satisfaction among patients. (dermatologyadvisor.com)
- Other options for topical therapy include iodine and salicylic acid, potassium hydroxide, tretinoin, cantharidin (a blistering agent usually applied in an office setting), and imiquimod (T cell modifier). (cdc.gov)
- Two experimental topical drugs, a new standardized preparation of topical cantharidin, called VP-102, and a topical nitric oxide (NO)-releasing product containing berdazimer, called SB206, represent promising products that have been designed to overcome the limitations of current treatments. (unict.it)
Beetle4
- In its natural form, cantharidin is secreted by the male blister beetle, and given to the female as a copulatory gift during mating. (wikipedia.org)
- Cantharidin, from the Greek kantharis, for beetle, is an odorless, colorless natural product with solubility in various organic solvents,[specify] but only slight solubility in water. (wikipedia.org)
- Males of Berberomeloe majalis have higher level of cantharidin per beetle: 64.22 ± 51.28 mg/g (dry weight) and 9.10 ± 12.64 mg/g (d. w. (wikipedia.org)
- The active ingredient in Spanish fly is supposedly a beetle called cantharidin. (adventurecostablanca.com)
Warts2
- Cantharidin, a naturally derived compound found in the Blusoms™ TagOutXpress Remover , offers an exceptional and natural approach to the removal of skin tags and warts. (neutroera.com)
- The substance cantharidin, which is found in Spanish Fly, is also used in medical treatments for warts. (adventurecostablanca.com)
Substance4
- Cantharidin is an odorless, colorless fatty substance of the terpenoid class, which is secreted by many species of blister beetles. (wikipedia.org)
- Cantharidin is classified as an extremely hazardous substance in the United States, and is subject to strict reporting requirements by facilities that produce, store, or use it in significant quantities. (wikipedia.org)
- This secretion contains cantharidin, an irritating substance that can cause blistering on human skin. (whatsthatbug.com)
- However, it's worth noting that using Spanish Fly can be dangerous and potentially harmful, as it contains a substance called cantharidin that can cause serious health problems. (adventurecostablanca.com)
Beetles3
- The level of cantharidin in blister beetles can be quite variable. (wikipedia.org)
- However, oil beetles do not bite or sting, and their primary defense mechanism is the release of cantharidin. (whatsthatbug.com)
- The largely herbivorous spur-wing goose of Africa sometimes has poison in its body, perhaps from eating blister beetles, which contain the potent toxins cantharidin. (juneauempire.com)
Efficacy1
- As the days pass, the treated area may form a blister, indicating the efficacy of Cantharidin in targeting the skin growth. (neutroera.com)
Spanish Fly1
- Spanish Fly, Cantharidin, Canth. (abchomeopathy.com)
Bandage1
- After cantharidin is applied, the area is covered with a bandage. (bestonlinemd.com)
Medications1
- Cantharidin is in a class of medications called vesicants. (medlineplus.gov)
Horses2
- Poisoning from cantharidin is a significant veterinary concern, especially in horses, but it can also be poisonous to humans if taken internally (where the source is usually experimental self-exposure). (wikipedia.org)
- Horses with cantharidin toxicosis develop colic, decreased appetite, depression and sweating, blood in the urine, dark mucous membranes, increased heart rate and respiratory rate and low blood calcium. (vin.com)
Skin3
- Cantharidin comes as a solution (liquid) to apply to the skin by a healthcare professional at a doctor's office or clinic. (medlineplus.gov)
- For example, when squeezed or distressed, the cantharidin in the excreted oil may cause skin irritation and blisters for people who have sensitive skin or allergies. (whatsthatbug.com)
- Harnessing the power of tea tree oil and Cantharidin , this advanced formula offers a safe and gentle approach to removing unwanted skin growths. (neutroera.com)
Blistering agent1
- Externally, cantharidin is a potent vesicant (blistering agent), exposure to which can cause severe chemical burns. (wikipedia.org)
Treatment1
- Cantharidin 0.7% could be an emerging standard for molluscum treatment. (dermatologytimes.com)
Harmful1
- Cantharidin has the potential to be harmful to pets, particularly if ingested. (whatsthatbug.com)
Drug1
- The Pharmacy Compounding Advisory Committee of the US Food and Drug Administration (FDA) voted yesterday to add squaric acid dibutyl ester, diphenylcyclopropenone, and cantharidin to its bulk drug substances list but voted not to add piracetam to the list. (medscape.com)
Single-use applicator3
- Ycanth is a drug-device combination product applied by a health care professional that delivers cantharidin, a blistering agent, in purple liquid via a single-use applicator. (primetherapeutics.com)
- Verricaʼs lead product candidate, VP-102, is a proprietary drug-device combination that contains a GMP-controlled formulation of cantharidin (0.7% w/v) delivered via a single-use applicator that allows for precise topical dosing and targeted administration. (researchandmarkets.com)
- White explained that VP-102 is designed for targeted administration of cantharidin through a topical GMP-controlled formulation through a single-use applicator. (dermatologytimes.com)
Verrica Pharmaceuticals2
- Verrica Pharmaceuticals announced that the US Food and Drug Administration (FDA) has accepted its resubmitted New Drug Application (NDA) for VP-102 (cantharidin 0.7%) for the treatment of molluscum contagiosum after 3 Complete Response Letters (CRL). (dermatologytimes.com)
- Cantharidin Verrica Pharmaceuticals can help get rid of common viral skin lesions. (biopharma.media)
Topical solution1
- tell your doctor and pharmacist if you are allergic to cantharidin, any other medications, or any of the ingredients in cantharidin topical solution. (medlineplus.gov)
Molluscum2
- It is not known exactly how cantharidin works to treat molluscum contagiosum. (medlineplus.gov)
- Compounded cantharidin has been used in the past to treat molluscum. (primetherapeutics.com)
Blister beetle3
- In its natural form, cantharidin is secreted by the male blister beetle, and given to the female as a copulatory gift during mating. (wikipedia.org)
- Cantharidin is the dried extract of the blister beetle (also termed Spanish fly). (medscape.com)
- As in the blister beetle, the active component is cantharidin. (21orover.com)
Toxic substance2
- Blister beetles contain a toxic substance, cantharidin, that causes irritation and ulceration in the horse's intestine. (holistichorse.com)
- The Spanish fly produces a toxic substance called cantharidin. (medikartindia.com)
Concern2
- Poisoning from cantharidin is a significant veterinary concern, especially in horses, but it can also be poisonous to humans if taken internally (where the source is usually experimental self-exposure). (wikipedia.org)
- Product production of the cantharidin treatment did not concern the FDA, but instead the overall quality of the CMO location. (dermatologytimes.com)
Solution2
- Cantharidin comes as a solution (liquid) to apply to the skin by a healthcare professional at a doctor's office or clinic. (medlineplus.gov)
- Cantharidin is the most common solution used to treat the lesions in the provider's office. (nih.gov)
Spanish1
- Spanish Fly, Cantharidin, Canth. (abchomeopathy.com)
Content1
- Cantharidin content in haemolymph is also higher in males (80.9 ± 106.5 µg/g) than in females (20.0 ± 41.5 µg/g). (wikipedia.org)
Active2
- Galangin, genistein, daidzein, and diosmin were active only in Hepa-1 cells, and cantharidin induced activity only in human HepG2 and MCF-7 cells. (nih.gov)
- The beetle, which thrives on plants of the families Oleaceae and Caprifoliaceae, contains 0.5-1 % of the active ingredient cantharidin. (21orover.com)
Doctor1
- If you become pregnant while receiving topical cantharidin, call your doctor. (medlineplus.gov)
Product1
- Cantharidin, from the Greek kantharis, for beetle, is an odorless, colorless natural product with solubility in various organic solvents,[specify] but only slight solubility in water. (wikipedia.org)
Application1
- Topical cantharidin may cause blistering or severe pain at the application site. (medlineplus.gov)
Store1
- Cantharidin is classified as an extremely hazardous substance in the United States, and is subject to strict reporting requirements by facilities that produce, store, or use it in significant quantities. (wikipedia.org)