CZ2012164A3 - Polymerní kompozice s ko-kontinuální strukturou, zejména k príprave implantátu se zvýsenou biokompatibilitou - Google Patents
Polymerní kompozice s ko-kontinuální strukturou, zejména k príprave implantátu se zvýsenou biokompatibilitou Download PDFInfo
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Abstract
Polymerní kompozice s ko-kontinuální strukturou je tvorena vzájemne propojenou kontinuální strukturou nosného skeletu a kontinuální strukturou biresorbovatelné výplne, pricemz nosný skelet je na bázi alespon jednoho bioinertního polymeru a bioresorbovatelná výpln je na bázi alespon jednoho polymeru hydrolyticky anebo enzymaticky rozlozitelného v prostredí zivých organismu, a zároven hmotnostní pomer nosného skeletu a bioresorbovatelné výplne je 20:80 az 80:20. Polymerní kompozice má s výhodou nosný skelet vytvoren na bázi polyolefinu, polyuretanu, polyesteru, vinylových polymeru, polymethylmethakrylátu a/nebo jejich kopolymeru. Bioresorbovatelná výpln pak je s výhodou tvorena materiálem na bázi polylaktidu a/nebo jeho kopolymeru, polyanhydridu, skrobu a/nebo jeho derivátu a ve vode rozpustných polymeru - polyethylenglykolu, polypropylenglykolu, polyvinylalkoholu a/nebo polyvinyl-pyrrolidonu.
Description
Polymerni kompozice s ko-kontinuâlni strukturou, zejména k pripravë implantâtù se zvÿsenou biokompatibilitou
Oblast techniky
Vynâlez se tÿkâ polymerni kompozice s ko-kontinuâlni strukturou, urcené zejména k pfipravé/ùpravë implantâtù se zvÿsenou biokompatibilitou a dale s moznosti fizeného uvolùovâni biologicky aktivnich lâtek. Reseni je urceno pro vyuziti v humânni a veterinâmi medicine.
Dosavadni stav techniky
Polymerni implantâty pro ortopedické a dentâlni aplikace Ize rozdèlit z pohledu jejich interakce s zivÿm organismem do dvou skupin. Prvni skupina — bioinertni implantâty — je vyrobena z polymerù, které bëhem jejich pfitomnosti v organismu nepodléhaji chemické dekompozici a plni tedy svùj ùëel v pùvodnim stavu, tvaru a velikosti, za nezmënënÿch mechanickÿch vlastnosti. Druhâ skupina — resorbovatelné implantâty — je pfipravena z materiâlù, které mohou bÿt organismem resorbovâny, pfiëemz jsou postupnë nahrazovâny tkâni, jejiz funkci docasnë pfevzaly.
Polymerni implantâty prvni skupiny pfedstavuji jako takové jednodussi reseni, protoze vsak nejsou ve srovnâni napfiklad s titanovÿmi implantâty zcela inertni co do pûsobeni na okolni tkân, pfi dlouhodobém kontaktu muze dochâzet ke zhorsené kompatibilitë materiâlù implantâtù s vlastni tkâni organismu a tim k nezâdoucim komplikacim.
Druhâ skupina - resorbovatelné implantâty - je vÿhodnâ vzhledem k moznosti postupného totâlm'ho odbourâni doëasné nâhrady - implantâtù - z tëla pacienta, coz je vnëkterÿch aplikacich velmi zâdoucf. Nevÿhodou tëchto implantâtù vsak je tëzko odhadnutelnÿ vÿvoj degradace a souvisejicich zmën mechanickÿch vlastnosti vlastniho implantâtù, coz mùze mit z hlediska jeho funkce fatâlni dûsledky.
Vzhledem k vÿse uvedenÿm skuteënostem se objevuji snahy vyhovët soucasnë pozadavkùm na mechanickou pevnost i potrebë bezproblémového zaëlenëni implantâtù do tëlniho prostredi. Z tëchto dùvodù se voli jako materiâl implantâtù polymery, které jsou biokompatibilni a pfitom v prostredi organismu dostatecnë stabilm, tedy bioinertni nebo s velmi pomalou biodegradaci, a jejich zakomponovâni do organismu je posileno pomoci pôrovité struktury, do niz pak postupnë prorùstâ tëlni tkân. Toto reseni je v mnoha ohledech vÿhodné, jeho urëitÿm nedostatkem je pokles mechanické pevnosti a dalsich dùlezitÿch fyzikâlnë mechanickÿch vlastnosti, které s sebou nese vytvoreni pôrovité struktury.
Podstata vynâlezu
Uvedené nevÿhody a nedostatky dosud znâmÿch feseni polymemich implantâtù, urcenÿch pfedevsim pro ortopedické a dentâlni aplikace, do znacné miry odstranuje polymemi kompozice s ko-kontinuâlni strukturou, zejména k pfipravë/ùpravë implantâtù se zvÿsenou biokompatibilitou, podle vynâlezu. Podstata vynâlezu spocivâ v tom, ze polymemi kompozice je tvofena vzâjemnë propojenou kontinuâlni strukturou nosného skeletu a kontinuâlni strukturou biresorbovatelné vÿplnë, pficemz nosnÿ skelet je na bâzi alespon jednoho bioinertniho polymeru a bioresorbovatelnâ vÿpln je na bâzi alespon jednoho polymeru hydrolyticky anebo enzymaticky rozlozitelného v prostfedi zivÿch organismù, a ’ Λ zâroven hmotnostni pomër nosného skeletu a bioresorbovatelné vÿplnë je 20|:j80 az 80:20
Polymemi kompozice s ko-kontinuâlni strukturou podle vynâlezu mâ s vÿhodou nosnÿ skelet vytvofen na bâzi polyolefinù, polyuretanù, polyesterû, vinylovÿch polymerû, polymetylmetakrylâtu a/nebo jejich kopolymerû. Bioresorbovatelnâ vÿpln pak je s vÿhodou na bâzi polylaktidu a/nebo jeho kopolymerû, polyanhydridû, skrobu a/nebo jeho derivâtù a ve vodë rozpustnÿch polymerû - polyetylénglykolu, polypropylenglykolu, polyvinylalkoholu a/nebo polyvinyl-pyrrolidonu.
Polymemi kompozice podle vynâlezu mûze mit v bioresorbovatelné vÿplni zaclenënou biologicky aktivni komponentu, napfiklad na bâzi pfirodnich antibiotik, silic a/nebo aromatickÿch extraktû z prirodnich materiâlù.
Polymemi kompozice podle vynâlezu mûze bÿt pouzita nejen jako samonosnÿ materiâl tvorici tëlo implantâtù, ale mûze bÿt rovnëz aplikovâna jako biokompatibilni povrchovâ vrstva na bëzném implantâtù tvofeném bioinertnim polymerem, kovem a/nebo keramikou.
Polymemi kompozice podle vynâlezu umoznuje zvÿseni biokompatibility implantâtù z ni vyrobenÿch diky tomu, ze je charakteristickâ dvëma spojitÿmi a navzâjem propojenÿmi fâzemi - nosnÿm skeletem a bioresorbovatelnou vÿplni. V pfipadë implantâtù vyrobeného z takové kompozice dochâzi v prostfedi zivého organismù postupnë k selektivni degradaci a resorpci kontinuâlni bioresorbovatelné vÿplnë. Prostor, kterÿ byl pûvodnë zaujimân bioresorbovatelnou vÿplni, pak tvofi spojité dutiny vnosném skeletu, které mohou bÿt posléze nahrazeny tkâni vrûstajici do porézni struktury novë vzniklé zpùvodnë celistvého implantâtù. Zbÿvajici porézni a postupnë zaplnovanÿ nosnÿ skelet pak pûsobi jako mechanickâ podpora pro novë vzniklÿ tkâni prorùstajici ùtvar.
Polymemi kompozice podle vynâlezu jsou velmi dobfe vyuzitelné pfedevsim v dentâlni chirurgii, kdy dochâzi k zachovâni mechanickÿch vlastnosti implantâtu a zâroven k resorpci velké ëâsti jeho hmoty a nahrazeni zivou tkâni.
Dalsi aditivni vÿhody polymerni kompozice podle vynâlezu pak nabÿvaji na vÿznamu v pfipadech, kdy je navic do bioresorbovatelné vÿplnë selektivnë inkorporovâna bioaktivni komponenta, kterâ bude pak bëhem procesu degradace a resorpce vÿplnë uvolnovâna do okolniho tkânového prostfedi. Kromë zvÿseni kompatibility dané prorùstânim tkânë dovnitf implantâtu pak Ize ocekâvat také podpùmÿ asimilaëni ci lécebnÿ ùëinek vlivem postupného uvolnovâni bioaktivni slozky, coz urychli procès hojeni v mistë implantace a také zamezi moznÿm negativnim interakcim zpùsobenÿch vlivem operacniho ùkonu, odezvy na implantât jako takové nebo pfipadné nozokomiâlni infekce.
Pfehled obrâzkù na vykresech
Kblizsim objasnëni podstaty vynâlezu slouzi pfiklad polymemi kompozice s kokontinuâlni strukturou, znâzomënou na pfilozenÿch vÿkresech, kde obr. 1 pfedstavuje snimek z elektronového mikroskopu, zachycujici strukturu nosného skeletu na bâzi polyamidu 6 (PA6) po selektivnim odstranëni bioresorbovatelné vÿplnë na bâzi polylaktidu (PLA), jak je popsâno v pfikladu 1. Obr. 2 pfedstavuje analogickÿ snimek struktury nosného skeletu na bâzi nizkohustotniho polyetylénu (LDPE), coz odpovidâ pfikladu 2.
Pfiklady nrovedeni vynâlezu
Priklad 1
Byly pfipraveny câstecnë rozlozitelné polymemi kompozice na bâzi polyamidu 6 (PA6) a polymeru kyseliny mléëné (PLA) vrùznÿch koncentracnich pomërech v koncentracnim rozmezi 50\60 hmotn. % PLA. Jednotlivé kompozice PA6/PLA byly podrobeny analÿze na detekci vzniku ko-kontinuâlni struktury. Plnë rozvinutâ ko-kontinuâlni struktura PA6/PLA byla nalezena u kompozice o hmotnostnim pomëru PA6/PLA 40/60 - viz obr. 1.
Priklad 2
Byly pfipraveny câstecnë rozlozitelné polymemi smësi na bâzi nizkohustotniho polyetylénu (LDPE) a polymeru kyseliny mlécné (PLA) v rùznÿch koncentracnich pomërech. Jednotlivé kompozice LDPE/PLA byly podrobeny analÿze na detekci vzniku ko-kontinuâlni struktury. Plnë rozvinutâ ko-kontinuâlni struktura LDPE/PLA byla nalezena u kompozice o hmotnostnim pomëru 50/50 - viz obr. 2.
Byly pfipraveny polymemi kompozice die pfikladu 1 s tim rozdilem, ze navic obsahovaly 1 hmotn. % krystalové violeti (CV), vztazeno na celkovou hmotnost obou polymerù. Takto pfipravené smësi byly podrobovâny hydrolytické degradaci pfi rùznÿch pH (3, 7, 9) a byla sledovâna koncentrace uvolnëné CV. Vÿsledky ukâzaly, ze maximâlni mnozstvi CV bylo uvolnèno z kompozice vykazujici ko-kontinuâlni strukturu detekovanou v prikladu 1.
P f i k 1 a d 4
Byly pfipraveny polymerni kompozice die prikladu c. 2 s tim rozdilem, ze navic obsahovaly 1 hmotn. % krystalové violeti (CV), vztazeno na celkovou hmotnost obou polymerù. Takto pfipravené smësi byly podrobovâny hydrolytické degradaci pfi rùznÿch pH (3, 7, 9) a byla sledovâna koncentrace uvolnëné CV. Vÿsledky ukâzaly, ze maximâlni mnozstvi CV bylo uvolnëno z kompozice vykazujici ko-kontinuâlni strukturu detekovanou v pfikladu 2.
Prùmyslovâ vyuzitelnost
Polymemi kompozice s ko-kontinuâlni strukturou podle vynâlezu je vyuzitelnâ zejména v humânni a veterinâmi medicinë. Pfedstavuje materiâl s vlastnostmi pfedurcujicimi jej kpfipravë implantâtù se zvÿsenou biokompatibilitou. Pfitomnosti bioresorbovatelné slozky je zâroven mozno vyuzit k fizenému uvolnovâni biologicky aktivnich lâtek.
Claims (5)
- wi ' PATENTOVÉ N À R O K Y1. Polymemi kompozice s ko-kontinuâlni strukturou, zejména k pfipravë/ùpravë implantâtû se zvÿsenou biokompatibilitou, vyznacujici se t i m,ze je tvofena vzâjemnë propojenou kontinuâlni strukturou nosného skeletu a kontinuâlni strukturou biresorbovatelné vÿplnë, pfiëemz nosnÿ skelet je na bâzi alespon jednoho bioinertniho polymeru a bioresorbovatelnâ vÿpln je na bâzi alespon jednoho polymeru hydrolyticky anebo enzymaticky rozlozitelného v prostfedi zivÿch organismù, a zâroven hmotnostni pomër nosného skeletu a bioresorbovatelné vÿplnë je 20 : 80 az 80 : 20.
- 2. Polymemi kompozice podle nâroku 1,vyznacujici se ti m, ze nosnÿ skelet je na bâzi polyolefmù, polyuretanù, polyesteru, vinylovÿch polymeru, polymetylmetakrylâtu a/nebo jejich kopolymerù.
- 3. Polymemi kompozice podle nâroku 1, vyznacujici se tim, ze bioresorbovatelnâ vÿpln je na bâzi polylaktidu a/nebo jeho kopolymerù, polyanhydridù, skrobu a/nebo jeho derivâtu a ve vodë rozpustnÿch polymerù — polyetylénglykolu, polypropylenglykolu, polyvinylalkoholu a/nebo polyvinylpyrrolidonu.
- 4. Polymemi kompozice podle nâroku 1, vy zn a ë u j i c i se t i m, ze bioresorbovatelnâ vÿpln obsahuje biologicky aktivni komponentu, zejména na bâzi pfirodnich antibiotik, silic a/nebo aromatickÿch extraktù z phrodnich materiâlù.
- 5. . olymemi kompozice podle nâroku 1, vy zn a c u j i c i se t i m, ze polymemi kompozice tvofi biokompatibilni povrchovou vrstvu na bëzném implantâtû tvoreném bioinertnim polymerem, kovem a/nebo keramikou.
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| Application Number | Priority Date | Filing Date | Title |
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| CZ20120164A CZ2012164A3 (cs) | 2012-03-08 | 2012-03-08 | Polymerní kompozice s ko-kontinuální strukturou, zejména k príprave implantátu se zvýsenou biokompatibilitou |
| PCT/CZ2013/000030 WO2013131499A1 (en) | 2012-03-08 | 2013-03-08 | Polymeric composite with co-continual structure, especially for the preparation of implants with the increased bio-compatibility |
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| CZ (1) | CZ2012164A3 (cs) |
| WO (1) | WO2013131499A1 (cs) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK201700367A1 (en) * | 2017-06-21 | 2019-01-30 | Jonsman Innovation Aps | A hydrophilic polymeric material |
| CZ310422B6 (cs) * | 2021-04-15 | 2025-06-04 | Centrum organické chemie s.r.o | Způsob přípravy termoplastu s disipativními či antistatickými vlastnostmi modifikovaného vodivými polymery |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3797499A (en) * | 1970-05-13 | 1974-03-19 | Ethicon Inc | Polylactide fabric graphs for surgical implantation |
| US5080665A (en) * | 1990-07-06 | 1992-01-14 | American Cyanamid Company | Deformable, absorbable surgical device |
| DE4216496C2 (de) * | 1992-05-19 | 1994-09-22 | Werner Prof Dr Med Sattel | Verwendung eines Plombenkörpers zum Einsetzen in eine Knochenhöhle, insbesondere in den Markraum eines Röhrenknochens |
| US6514535B2 (en) * | 1999-05-21 | 2003-02-04 | Noveon Ip Holdings Corp. | Bioadhesive hydrogels with functionalized degradable crosslinks |
| GB0202233D0 (en) * | 2002-01-31 | 2002-03-20 | Smith & Nephew | Bioresorbable polymers |
| AU2003245424A1 (en) * | 2002-06-06 | 2003-12-22 | Rutgers, The State University | Co-continuous phase composite polymer blends for in-vivo and in-vitro biomedical applications |
| US7951436B2 (en) * | 2006-08-14 | 2011-05-31 | Frito-Lay North America, Inc. | Environmentally-friendly multi-layer flexible film having barrier properties |
| GB0822892D0 (en) * | 2008-12-16 | 2009-01-21 | Univ Nottingham | Degradable composite |
-
2012
- 2012-03-08 CZ CZ20120164A patent/CZ2012164A3/cs unknown
-
2013
- 2013-03-08 WO PCT/CZ2013/000030 patent/WO2013131499A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| CZ303996B6 (cs) | 2013-08-07 |
| WO2013131499A1 (en) | 2013-09-12 |
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