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MD4341C1 - Syrup for the treatment of gastric precancerous conditions - Google Patents

Syrup for the treatment of gastric precancerous conditions Download PDF

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Publication number
MD4341C1
MD4341C1 MDA20130088A MD20130088A MD4341C1 MD 4341 C1 MD4341 C1 MD 4341C1 MD A20130088 A MDA20130088 A MD A20130088A MD 20130088 A MD20130088 A MD 20130088A MD 4341 C1 MD4341 C1 MD 4341C1
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Moldova
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vitamin
syrup
treatment
nanoparticles
precancerous conditions
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MDA20130088A
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Romanian (ro)
Russian (ru)
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MD4341B1 (en
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Ион МЕРЕУЦЭ
Владимир ВАЛИКА
Владимир КАРАУШ
Серджиу ПАРИЙ
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Ион МЕРЕУЦЭ
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Publication of MD4341C1 publication Critical patent/MD4341C1/en

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Abstract

The invention relates to gastroenterology, in particular to biologically active substances in the form of syrups, which can be used for the treatment of gastric precancerous conditions.According to the invention, the claimed syrup comprises: vitamin A, vitamin D2, vitamin E, vitamin C, vitamin B1, vitamin B2, niacin, vitamin B6, vitamin B12, biotin, folic acid, pantothenic acid, magnesium oxide, copper oxide, sodium selenate, nanoparticles of zinc oxide and silver, taken in the ratio of 9:1, and sugar syrup, in the following quantitative ratio of components per 100 ml:

Description

Invenţia se referă la gastroenterologie, în special la substanţe biologic active în formă de siropuri care pot fi utilizate pentru tratamentul stărilor precanceroase gastrice. The invention relates to gastroenterology, in particular to biologically active substances in the form of syrups that can be used for the treatment of gastric precancerous conditions.

Se cunoaşte că depistarea şi tratamentul stărilor precanceroase ale stomacului reprezintă profilaxia secundară a cancerului gastric (Беспалов В. Г. Индивидуальная профилактика рака. Питер, 2001, с. 123-126). It is known that the detection and treatment of pre-cancerous conditions of the stomach represent the secondary prophylaxis of gastric cancer (Беспалов В. Г. Индивидеольная профилактия рака. Питер, 2001, с. 123-126).

În prezent la principalele stări precanceroase ale stomacului se referă gastrita cronică atrofică şi infectarea cu Helicobacter pylori, iar la schimbările precanceroase principale se referă metaplazia intestinală şi displazia intestinală a epiteliului gastric (Аруин Л. И., Капуллер Л. Л., Исаков В. А. Морфологическая диагностика желудка и кишечника. Москва, Триада-Х, 1998, с. 269-300). Currently, chronic atrophic gastritis and Helicobacter pylori infection are the main precancerous conditions of the stomach, and intestinal metaplasia and intestinal dysplasia of the gastric epithelium are the main precancerous changes (Аруин Л. И., Капуллер Л. Л., Исаков В. A. Morphological diagnosis of the stomach and intestines. Moscow, Triada-X, 1998, pp. 269-300).

Este cunoscută metoda de tratament al stărilor precanceroase gastrice, care constă în aceea că se administrează un remediu medicamentos care conţine decoct din flori de tei şi din partea aeriană de vâsc alb, amestec din mediul de cultură RPMI 1640 şi celule stem, extract proteic din ţesut tumoral, în următorul raport al componentelor, în % mas.: decoct din flori de tei 10, decoct din partea aeriană de vâsc alb 20, amestec din mediul de cultură RPMI 1640 şi celule stem 35, extract proteic din ţesut tumoral 35, administrarea se efectuează per os, de 4…5 ori pe zi, cu 30 min înainte de masă, cate 20 ml, timp de 60…120 zile [1]. There is a known method of treating gastric precancerous conditions, which consists in the administration of a medicinal remedy containing a decoction of linden flowers and the aerial part of white mistletoe, a mixture of RPMI 1640 culture medium and stem cells, protein extract from tissue tumor, in the following ratio of the components, in mass %: decoction of linden flowers 10, decoction of the aerial part of white mistletoe 20, mixture of culture medium RPMI 1640 and stem cells 35, protein extract from tumor tissue 35, the administration is perform orally, 4...5 times a day, 30 min before meals, 20 ml each, for 60...120 days [1].

Dezavantajul acestei metode constă în aceea că este complicată în vederea obţinerii remediului medicamentos şi poate provoca reacţii alergice la pacienţii cu astm bronşic. The disadvantage of this method is that it is complicated in order to obtain the medicinal remedy and can cause allergic reactions in patients with bronchial asthma.

Mai este cunoscută metoda de tratament al stărilor precanceroase gastrice, care constă în aceea că se administrează remediul KLAMIN (concentrat din Laminaria saccharina L. Lamour), obţinut din fracţia lipidică a algelor brune de mare, câte 2 pastile de trei ori pe zi, cu 15…30 min înainte de masă, timp de 6 luni, cu repetarea curei de tratament peste 1…3 luni [2]. There is also a known method of treating gastric precancerous conditions, which consists in administering the remedy KLAMIN (concentrate from Laminaria saccharina L. Lamour), obtained from the lipid fraction of brown seaweed, 2 pills three times a day, with 15...30 min before meals, for 6 months, with the repetition of the treatment course after 1...3 months [2].

Dezavantajul acestei metode constă în aceea că remediul KLAMIN conţine iod, din care cauză este contraindicat persoanelor care suferă de tireotoxicoză, insuficienţă renală şi hepatică cronică. The disadvantage of this method is that the KLAMIN remedy contains iodine, which is why it is contraindicated for people suffering from thyrotoxicosis, chronic kidney and liver failure.

Se cunoaşte de asemenea o metodă de tratament al stărilor precanceroase gastrice, care constă în aceea că se administrează per os o compoziţie care conţine vitamina E şi β-caroten [3]. A method is also known for the treatment of gastric precancerous conditions, which consists in the fact that a composition containing vitamin E and β-carotene is administered orally [3].

Dezavantajul acestei metode constă în aceea că compoziţia se administrează timp îndelungat, devenind posibilă cumularea vitaminei liposolubile în organism, ceea ce poate duce la manifestarea unui şir de efecte adverse. The disadvantage of this method is that the composition is administered for a long time, making it possible to accumulate the fat-soluble vitamin in the body, which can lead to the manifestation of a series of adverse effects.

Este cunoscut un supliment alimentar, denumit şi „Vidaylin-m - sirop”, administrat în patologiile gastro-intestinale pentru tratamentul gastritei cronice atrofice ce conţine: retinol (vitamina A - sub formă de palmitat) 0,9 mg (3000 UI, ergocalciferol (vitamina D2) 10 mg (400 UI), tiamină (vitamina B1 - sub formă de clorhidrat) 1,5 mg, riboflavină (vitamina B2 - sub formă de riboflavina-5-sodiu fosfat) 1,2 mg, piridoxină (vitamina B6 - sub formă de clorhidrat) 1 mg, ciancobalamină (vitamina B12) 3 mg, acid ascorbic (vitamina C) 50 mg, nicotinamidă 10 mg, pantenol 5 mg, fosfor (sub formă hipofosfat de calciu şi acid hipofosforic) 43 mg, calciu (sub formă de lactat de calciu şi hipofosfat de calciu) 40 mg, magneziu (sub formă de gluconat de magneziu) 3 mg, zinc (sub formă de glucoheptonat de zinc) 0,5 mg, iod (sub formă de iodură de potasiu) 75 mg, mangan (sub formă de gluconat de mangan) 0,5 mg, fier (sub formă de Fe II-gluconat) 3 mg, colină (sub formă de bitartrat de colină) 5 mg, ionozitol 5 mg [4]. A food supplement is known, also called "Vidaylin-m - syrup", administered in gastrointestinal pathologies for the treatment of chronic atrophic gastritis, which contains: retinol (vitamin A - in the form of palmitate) 0.9 mg (3000 IU, ergocalciferol ( vitamin D2) 10 mg (400 IU), thiamine (vitamin B1 - in the form of hydrochloride) 1.5 mg, riboflavin (vitamin B2 - in the form of riboflavin-5-sodium phosphate) 1.2 mg, pyridoxine (vitamin B6 - as hydrochloride) 1 mg, cyanocobalamin (vitamin B12) 3 mg, ascorbic acid (vitamin C) 50 mg, nicotinamide 10 mg, panthenol 5 mg, phosphorus (as calcium hypophosphate and hypophosphoric acid) 43 mg, calcium (as form of calcium lactate and calcium hypophosphate) 40 mg, magnesium (as magnesium gluconate) 3 mg, zinc (as zinc glucoheptonate) 0.5 mg, iodine (as potassium iodide) 75 mg , manganese (in the form of manganese gluconate) 0.5 mg, iron (in the form of Fe II-gluconate) 3 mg, choline (in the form of choline bitartrate) 5 mg, ionositol 5 mg [4].

Dezavantajul acestui supliment constă în aceea că are o acţiune insuficientă asupra evoluţiei gastritei cronice atrofice şi chiar la administrări îndelungate (timp de 8 luni) nu produce efecte semnificative de tratament, adică la fibrogastroscopie se atestă atrofia mucoasei gastrice, dar pe suprafaţe mai mici faţă de cele determinate înainte de tratament, totodată contribuie la cumularea vitaminelor liposolubile în organism, ceea ce duce la manifestarea unui şir de efecte adverse. The disadvantage of this supplement is that it has insufficient action on the evolution of chronic atrophic gastritis and even with prolonged administration (for 8 months) it does not produce significant treatment effects, i.e. at fibrogastroscopy atrophy of the gastric mucosa is attested, but on smaller surfaces compared to those determined before the treatment, also contribute to the accumulation of fat-soluble vitamins in the body, which leads to the manifestation of a series of adverse effects.

În ultimul deceniu au fost efectuate mai multe cercetări în domeniul structurilor de carbon, îndeosebi a nanoparticulelor de carbon şi microcorpusculilor de 1…10 nm. Pentru prima dată nanoparticulele de carbon au fost sintetizate în 1963 şi au fost aplicate în diverse tehnologii industriale. Semnificativ este faptul că în procesul activităţii acestor nanoparticule are loc degajarea de căldură. In the last decade, several researches were carried out in the field of carbon structures, especially carbon nanoparticles and microcorpuscles of 1...10 nm. For the first time carbon nanoparticles were synthesized in 1963 and were applied in various industrial technologies. It is significant that in the process of the activity of these nanoparticles heat is released.

O particularitate semnificativă a nanoparticulelor este că ele pătrund în membrana celulară şi pot precipita la suprafaţa sferică a mai multor celule substanţe biologic active, medicamente, polimeri etc. Aceste caracteristici au stat la baza aplicării nanoparticulelor cu scop de dezintoxicare şi în calitate de conductor. În aşa fel, în anul 2000 nanoparticulele au fost folosite la pacienţii oncologici care au fost supuşi radio- şi chimioterapiei, cu scop de dezintoxicare. A significant feature of nanoparticles is that they penetrate the cell membrane and can precipitate biologically active substances, drugs, polymers, etc. on the spherical surface of several cells. These characteristics were the basis for the application of nanoparticles for the purpose of detoxification and as a conductor. In this way, in the year 2000, nanoparticles were used in oncological patients who were subjected to radio- and chemotherapy, with the aim of detoxification.

Problema pe care o soluţionează invenţia propusă constă în crearea unui supliment alimentar în formă de sirop, care ar avea efecte vizibile în tratamentul stărilor precanceroase gastrice, ar reduce durata de tratament fără manifestarea unui şir de efecte adverse. The problem that the proposed invention solves consists in the creation of a food supplement in the form of syrup, which would have visible effects in the treatment of gastric precancerous conditions, would reduce the duration of treatment without the manifestation of a series of adverse effects.

Conform invenţiei, siropul revendicat conţine: vitamina A, vitamina D2, vitamina E, vitamina C, vitamina B1, vitamina B2, niacină, vitamina B6, vitamina B12, biotină, acid folic, acid pantoteic, oxid de magneziu, oxid de cupru, selenat de sodiu, nanoparticule de oxid de zinc şi argint, luate în raport de 9:1, şi sirop de zahăr, ingredientele fiind luate în următorul raport cantitativ pentru 100 ml: According to the invention, the claimed syrup contains: vitamin A, vitamin D2, vitamin E, vitamin C, vitamin B1, vitamin B2, niacin, vitamin B6, vitamin B12, biotin, folic acid, pantotheic acid, magnesium oxide, copper oxide, selenate of sodium, nanoparticles of zinc oxide and silver, taken in a ratio of 9:1, and sugar syrup, the ingredients being taken in the following quantitative ratio for 100 ml:

vitamina A, mg 0,8 vitamina D2, mg 0,005 vitamina E, mg 10 vitamina C, mg 100 vitamina B1, mg 3 vitamina B2, mg 3,6 niacină, mg 40 vitamina B6, mg 2 vitamina B12, mg 0,003 biotină, mg 0,06 acid folic, mg 0,2 acid pantoteic, mg 15 oxid de magneziu, mg 375 oxid de cupru, mg 1 selenat de sodiu, mg 0,055 nanoparticule de oxid de zinc şi argint, mg 6 sirop de zahăr, ml restul. vitamin A, mg 0.8 vitamin D2, mg 0.005 vitamin E, mg 10 vitamin C, mg 100 vitamin B1, mg 3 vitamin B2, mg 3.6 niacin, mg 40 vitamin B6, mg 2 vitamin B12, mg 0.003 biotin, mg 0.06 folic acid, mg 0.2 pantotheic acid, mg 15 magnesium oxide, mg 375 copper oxide, mg 1 sodium selenate, mg 0.055 nanoparticles of zinc oxide and silver, mg 6 sugar syrup, ml the rest .

Rezultatul invenţiei constă în obţinerea unui supliment alimentar în formă de sirop, care are efecte vizibile în tratamentul complet al stărilor precanceroase gastrice, timp de 3 luni, datorită selectării reuşite a vitaminelor şi a raportului lor în combinaţie cu microelementele şi nanoparticulele de oxid de argint şi de zinc luate în raport de 9:1, care pătrund mult mai uşor în celulele mucoasei. The result of the invention consists in obtaining a food supplement in the form of syrup, which has visible effects in the complete treatment of gastric precancerous conditions, for 3 months, due to the successful selection of vitamins and their ratio in combination with microelements and nanoparticles of silver oxide and of zinc taken in a ratio of 9:1, which penetrate much more easily into the cells of the mucosa.

Siropul nutriţional se prepară în felul următor. The nutritional syrup is prepared in the following way.

Ingredientele se selectează conform invenţiei, se cântăresc conform cantităţilor revendicate. Ingredientele se folosesc sub formă de pulbere. Apoi se prepară 100 ml de sirop din zahăr în felul următor: 64 g de zahăr se dizolvă în apă caldă de 70°C timp de 1…2 min, agitându-se permanent. Siropul se trece prin aparatul cu vapori-vid şi se pasteurizează în aparatul cu vapori-vid, timp de cel puţin 20 min, la temperatura de 98…100ºC. Apoi la ingredientele pregătite, care în total constituie 556,723 mg, se adaugă siropul pregătit şi răcit până la 20°C şi se malaxează timp de 10 min. Indicele de refracţie al siropului nutriţional trebuie să fie de 1,4486…1,4532. Caracteristicile organoleptice ale siropului sunt: netransparent, de culoare uşor gălbuie, cu miros specific şi gust dulce amărui. The ingredients are selected according to the invention, weighed according to the claimed quantities. The ingredients are used in powder form. Then prepare 100 ml of sugar syrup in the following way: dissolve 64 g of sugar in warm water at 70°C for 1...2 min, stirring constantly. The syrup is passed through the steam-vacuum machine and pasteurized in the steam-vacuum machine for at least 20 min, at a temperature of 98...100ºC. Then to the prepared ingredients, which in total constitute 556.723 mg, add the prepared syrup cooled to 20°C and mix for 10 min. The refractive index of the nutritional syrup must be 1.4486...1.4532. The organoleptic characteristics of the syrup are: non-transparent, slightly yellowish in color, with a specific odor and bittersweet taste.

Nanoparticulele de oxid de zinc şi de argint sunt luate în raport masic de 9:1 şi se obţin conform brevetului RU 2451578 C1 2012.05.27, totodată nanoparticulele menţionate, cât şi celelalte ingrediente pot fi procurate în reţeaua liberă de distribuţie a ingredientelor pentru fabricarea remediilor medicamentoase. The nanoparticles of zinc oxide and silver are taken in a mass ratio of 9:1 and are obtained according to the patent RU 2451578 C1 2012.05.27, at the same time the mentioned nanoparticles, as well as the other ingredients can be purchased in the free distribution network of ingredients for the manufacture of remedies medicines.

Condiţionarea siropului se efectuează în flacoane din tereftalat de polietilenă cu volumul de 100 ml şi se etanşează cu dopuri din polietilenă. The conditioning of the syrup is carried out in polyethylene terephthalate bottles with a volume of 100 ml and sealed with polyethylene caps.

Termenul de valabilitate - 3 ani, la temperatura de până la 25°C. Shelf life - 3 years, at a temperature of up to 25°C.

Exemplu concret de realizare Concrete example of realization

Pacienta A., 57 ani, acuze la eructaţie cu miros fetid, greutate în regiunea epigastrică, meteorism, dureri gastrice ce se intensifică după alimentaţie. FEGPS - mucoasa gastrică atrofică, pliurile mucoase sunt denivelate. Pacienta a primit tratament conform metodei revendicate, adică zilnic, per os, câte 100 ml de sirop nutriţional dimineaţa şi sera cu 20 min înainte de masă. Cura de tratament a constituit 3 luni. După aceasta, la investigaţiile efectuate ulterior s-a stabilit dispariţia semnelor clinice şi ameliorarea stării pacientei. Efecte adverse în cazul tratamentului efectuat conform metodei revendicate nu s-au manifestat. Pacienta a fost monitorizată pe parcursul unui an, recidive nu s-au depistat. Patient A., 57 years old, complains of belching with a fetid smell, heaviness in the epigastric region, flatulence, gastric pain that intensifies after eating. FEGPS - atrophic gastric mucosa, the mucosal folds are uneven. The patient received treatment according to the claimed method, i.e. daily, per os, 100 ml of nutritional syrup in the morning and in the evening 20 minutes before the meal. The treatment course was 3 months. After this, during the subsequent investigations, it was established that the clinical signs disappeared and the patient's condition improved. Adverse effects in the case of treatment carried out according to the claimed method did not appear. The patient was monitored for a year, no recurrences were detected.

Conform metodei revendicate au fost trataţi 18 pacienţi, reacţii adverse şi recidive nu s-au depistat. According to the claimed method, 18 patients were treated, adverse reactions and relapses were not detected.

1. MD 3972 C2 2010.08.31 1. MD 3972 C2 2010.08.31

2. RU 2034560 C1 1995.05.10 2. RU 2034560 C1 1995.05.10

3. WO 9102535 A1 1991.03.07 3. WO 9102535 A1 1991.03.07

4. Регистр лекарственных средств. Энциклопедия лекарств. Выпуск 21, 2012, p. 1426 4. Register of medicines. Encyclopedia of medicines. Issue 21, 2012, p. 1426

Claims (1)

Sirop pentru tratamentul stărilor precanceroase gastrice care conţine: vitamina A, vitamina D2, vitamina E, vitamina C, vitamina B1, vitamina B2, niacină, vitamina B6, vitamina B12, biotină, acid folic, acid pantoteic, oxid de magneziu, oxid de cupru, selenat de sodiu, nanoparticule de oxid de zinc şi argint, luate în raport de 9:1, şi sirop de zahăr, ingredientele fiind luate în următorul raport cantitativ pentru 100 ml:Syrup for the treatment of gastric precancerous conditions containing: vitamin A, vitamin D2, vitamin E, vitamin C, vitamin B1, vitamin B2, niacin, vitamin B6, vitamin B12, biotin, folic acid, pantotheic acid, magnesium oxide, copper oxide , sodium selenate, nanoparticles of zinc oxide and silver, taken in a ratio of 9:1, and sugar syrup, the ingredients being taken in the following quantitative ratio for 100 ml: vitamina A, mg 0,8 vitamina D2, mg 0,005 vitamina E, mg 10 vitamina C, mg 100 vitamina B1, mg 3 vitamina B2, mg 3,6 niacină, mg 40 vitamina B6, mg 2 vitamina B12, mg 0,003 biotină, mg 0,06 acid folic, mg 0,2 acid pantoteic, mg 15 oxid de magneziu, mg 375 oxid de cupru, mg 1 selenat de sodiu, mg 0,055 nanoparticule de oxid de zinc şi argint, mg 6 sirop de zahăr, ml restul. vitamin A, mg 0.8 vitamin D2, mg 0.005 vitamin E, mg 10 vitamin C, mg 100 vitamin B1, mg 3 vitamin B2, mg 3.6 niacin, mg 40 vitamin B6, mg 2 vitamin B12, mg 0.003 biotin, mg 0.06 folic acid, mg 0.2 pantotheic acid, mg 15 magnesium oxide, mg 375 copper oxide, mg 1 sodium selenate, mg 0.055 nanoparticles of zinc oxide and silver, mg 6 sugar syrup, ml the rest .
MDA20130088A 2013-11-21 2013-11-21 Syrup for the treatment of gastric precancerous conditions MD4341C1 (en)

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RU2473357C2 (en) * 2011-02-24 2013-01-27 Общество с ограниченной ответственностью "ДИНАМИК ДЕВЕЛОПМЕНТ ЛАБОРАТОРИЗ" Liquid composition improving working performance and possessing adaptogenic, wound-healing and anti-inflammatory action
CN103230431A (en) * 2013-04-27 2013-08-07 洪士炀 Medicine for treating stomach disease and application
CN103082299B (en) * 2012-12-26 2014-07-30 东莞市照燕生物科技有限公司 Nutritional healthcare product for clearing bowels and expelling toxin

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* Cited by examiner, † Cited by third party
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DE4032163C2 (en) * 1990-10-10 1995-03-30 Gradinger F Hermes Pharma S-retinoyl-L-aminomercapto compounds and intermediates, processes for their preparation and their use
DE4032187C2 (en) * 1990-10-10 1995-03-30 Gradinger F Hermes Pharma N-Retinoyl-L-aminomercapto compounds and intermediates, process for their preparation and their use
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CN1093402C (en) * 1998-08-11 2002-10-30 苏乐群 Gastritis treating tablet
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CN1698646A (en) * 2005-04-29 2005-11-23 朱舜时 Medicine composition for treating atrophic gastritis
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MD3972C2 (en) * 2009-03-11 2010-07-31 Ион МЕРЕУЦЭ Remedy and method for treating precancerous conditions
RU2473357C2 (en) * 2011-02-24 2013-01-27 Общество с ограниченной ответственностью "ДИНАМИК ДЕВЕЛОПМЕНТ ЛАБОРАТОРИЗ" Liquid composition improving working performance and possessing adaptogenic, wound-healing and anti-inflammatory action
CN103082299B (en) * 2012-12-26 2014-07-30 东莞市照燕生物科技有限公司 Nutritional healthcare product for clearing bowels and expelling toxin
CN103230431A (en) * 2013-04-27 2013-08-07 洪士炀 Medicine for treating stomach disease and application

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* Cited by examiner, † Cited by third party
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