N-Tense Topical is a synergistic formula similar to the popular N-Tense capsules.
N-Tense Topical can be applied directly on the skin as an adjuvant to traditional treatments of skin cancers that every year cause thousands of deaths.
Researches have documented as main cause of skin cancers the sunbeds or tanning lamps which consequently should be avoided. Moreover, it is recommended to apply a minumum of a factor 15 sunscreen at least 15-20 mins before going out into the sun. This sunscreen should be re-applied throughout the day. It's also strongly advised to stay out of the sun between 11am and 3pm when the suns rays are strongest.
Please note that N-Tense Topical cannot be used as sunscreen, nor can replace traditional skin cancer treatments.
All the products on Naturvitae.com are "HEF". To learn more, click here.
Why should I purchase N-Tense Topical? To learn more, click here.
Ingredients: 100% pure blend of sangre de grado, copaiba, graviola, espinheira santa, suma, bellaco caspi, huacapu, pau d'arco, mullaca, vassourinha, and mutamba extracted in distilled water and alcohol.
Suggested Use: Shake well and apply directly on the skin several times daily. Allow to dry completely before covering with clothing. For topical use only.
Other Practitioner Observations: This extract will stain clothing and other textiles.
Also Suggested:
- N-Tense, a proprietary blend of Rainforest botanicals with active properties
- Graviola Max, a blend of two species of graviola (Annona muricata&Annona monatna)
- Bellaco-caspi Extract, a plant form the Amazon used as a folk remedy against infections, women disorders (enometriosis, ovarian cysts, etc.), besides against cancer and tumors
References
Sangre de Grado (Croton lechleri)
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Copaiba Resin (Copaifera sp.)
Ohsaki, A., et al. “The isolation and in vivo potent antitumor activity of clerodane diterpenoids from the oleoresin of Brazilian medicinal plant Copaifera langsdorfii Desfon.” Bioorg. Med. Chem. Lett. 1994; 4: 2889–92.
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de Almeida Alves, T. M., et al. “Biological screening of Brazilian medicinal plants.”Mem. Inst. Oswaldo Cruz 2000; 95(3): 367–73.
Graviola (Annona muricata)
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Espinheira Santa (Maytenus ilicifolia)
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Buffa Filho, W., et al. “Quantitative determination for cytotoxic Friedo-nor-oleanane derivatives from five morphological types of Maytenus ilicifolia (Celastraceae) by reverse-phase high-performance liquid chromatography.” Phytochem. Anal. 2002 Mar-Apr; 13(2): 75-8.
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Suma (Pfaffia paniculata)
da Silva, T. C., et al. “Inhibitory effects of Pfaffia paniculata (Brazilian ginseng) on preneoplastic and neoplastic lesions in a mouse hepatocarcinogenesis model.” Cancer Lett. 2005 Aug; 226(2): 107-13.
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Bellaco-caspi (Himatanthus sucuuba)
Guignard, E., et al. "Screening of plants found in Amazonas state for lethality towards brine shrimp." Acta Amazonica. 2003; 33(1): 93-104.
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De Silva, J. R., et al. "Triterpenic esters from Himatanthus sucuuba (Spruce) Woodson." Quimica Nova 1998; 21(6): 702-704.
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Hamburger, M., et al. "Traditional medicinal plants of Thailand. XVII. Biologically active constituents of Plumeria rubra." J. Ethnopharmacol. 1991 Jul; 33(3): 289-92.
Huacapu (Minquartia guianensis)
Marles, R. J., et al. "Isolation of a novel cytotoxic polyacetylene from a traditional anthelmintic medicinal plant, Minquartia guianensis." J. Nat. Prod. 1989; 52(2): 261-266.
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Quignard, E. L. J., et al. "Medium lethal concentrations of amazonian plant extracts in the brine shrimp assay." Pharmaceutical Biology. 2004; 42(3): 253-257.
Rasmussem, H. B., et al. "Absolute configuration and antiprotozoal activity of minquartynoic acid." J. Nat. Prod. 2000; 63(9): 1295-1296.
Pau d'arco (Tabebuia impetiginosa)
Lee, J. H., et al. “Down-regulation of cyclooxygenase-2 and telomerase activity by beta-lapachone in human prostate carcinoma cells.” Pharmacol. Res. 2005; 51(6): 553-60.
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Park, H. J., et al. “Heat-induced up-regulation of NAD(P)H:quinone oxidoreductase potentiates anticancer effects of beta-lapachone.” Clin. Cancer Res. 2005 Dec; 11(24 Pt 1): 8866-71.
Balassiano, I. T., et al. “Demonstration of the lapachol as a potential drug for reducing cancer metastasis. Oncol. Rep. 2005; 13(2): 329-33
Choi, B. T., et al. “beta-Lapachone-induced apoptosis is associated with activation of caspase-3 and inactivation of NF-kappaB in human colon cancer HCT-116 cells.” Anticancer Drugs. 2003 Nov; 14(10): 845-50.
Renou, S. G., et al. “Monoarylhydrazones of alpha-lapachone: synthesis, chemical properties and antineoplastic activity.” Pharmazie. 2003 Oct; 58(10): 690-5.
Choi, Y. H., et al. “Suppression of human prostate cancer cell growth by beta-Lapachone via down-regulation of PRB phosphorylation and induction of Cdk Inhibitor p21(WAF1/CIP1).” J. Biochem. Mol. Biol. 2003 Mar; 36(2): 223-9.
Colman de Saizarbitoria, T., et al. “Bioactive furonaphtoquinones from Tabebuia barbata (Bignoniaceae).” Acta Cient. Venez. 1997; 48(1): 42-6.
Ueda, S., et al. “Production of anti-tumour-promoting furanonaphthoquinones in Tabebuia avellanedae cell cultures.” Phytochemistry. 1994 May; 36(2): 323-5.
Schuerch, A. R., et al. “B-Lapachone, an inhibitor of oncornavirus reverse transcriptase and eukarotic DBA polymerase-a. Inhibitory effect, thiol dependency and specificity.” Eur. J. Biochem. 1978; 84: 197–205.
Linardi, M. D. C., et al. “A lapachol derivative active against mouse lymphocyte leukemia P-388.” J. Med. Chem. 1975; 18(11): 1159–62.
Block, J. B., et al. “Early clinical studies with lapachol (NSC-11905).” Cancer Chemother. Rep. 1974; 4: 27–8.
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Mullaca (Physalis angulata)
Hsieh, W. T., et al. “Physalis angulata induced G2/M phase arrest in human breast cancer cells.” Food Chem Toxicol. 2006 Jan 18;
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Ismail, N., et al. “A novel cytotoxic flavonoid glycoside from Physalis angulata.” Fitoterapia. 2001 Aug. 72(6): 676–79
Chiang, H., et al. “Antitumor agent, physalin F from Physalis angulata L.” Anticancer Res. 1992; 12(3): 837–43.
Lee, W. C., et al. “Induction of heat-shock response and alterations of protein phosphorylation by a novel topoisomerase II inhibitor, withangulatin A, in 9L rat brain tumor cells.” Cell Physiol. 1991; 149(1): 66-67.
Juang, J. K., et al. “A new compound, withangulatin A, promotes type II DNA topoisomerasemediated DNA damage.” Biochem. Biophys. Res. Commun. 1989; 159(3): 1128–34.
Vassourinha (Scoparia dulcis)
Kasperczyk, H., et al. “Betulinic acid as new activator of NF-kappaB: molecular mechanisms and implications for cancer therapy.” Oncogene. 2005 Oct; 24(46): 6945-56.
Fulda, S., et al. “Sensitization for anticancer drug-induced apoptosis by betulinic acid." Neoplasia. 2005; 7(2):162-70
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Fulda, S., et al. “Betulinic acid induces apoptosis through a direct effect on mitochondria in neuroectodermal tumors.” Med. Pediatr. Oncol. 2000; 35(6): 616–18
Fulda, S., et al. “Betulinic acid: A new cytotoxic agent against malignant brain-tumor cells.” Int. J. Cancer 1999; 82(3): 435–41.
Noda, Y., et al. “Enhanced cytotoxicity of some triterpenes toward leukemia L1210 cells cultured in low pH media; possibility of a new mode of cell killing.” Chem. Pharm. Bull. 1997; 45(10): 1665–70.
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Mutamba (Guazuma ulmifolia)
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Nascimento, S. C., et al. “Antimicrobial and cytotoxic activities in plants from Pernambuco, Brazil.” Fitoterapia. 1990; 61(4): 353–55.
WARNINGS: Information, statements and products on this website have not been evaluated by the FDA and are not intended to diagnose, mitigate, treat, cure, or prevent any disease or health condition. The natural properties of the botanicals are only referred to their common uses among folk and herbal traditions. Our products are not intended to diagnose, cure, or prevent any disease as well. It's not meant to give any suggestion of diagnosis or disesase treatment. Please see a doctor when needed.