Documenti di Didattica
Documenti di Professioni
Documenti di Cultura
Biomaterial may be defined as a non living designed to interact with biological system Biocompatibility is the ability to elicit an appropriate biological response in a given application in the body Biological response will changes in the host, the application material, material its self A materials may be said to be biocompatible when it has the quality of being non destructive in the biological environtment
A single material may not be acceptable in all application Possible interaction between material and environment: - postoperative sensitivity - toxicity - hypersensitivity/allergic - corrosion In the development of any biomaterial must be consider: - strength - esthetic - functional & biocompatibility
Measuring Biocompatibility
Is not simple About the interactions between dental material oral tissue and technologies for testing improve Must be extensively screened for biocompatibility before are used in human
- in vitro (primary test, initials test) - animal (in vivo, secondary test) - usage test
In vitro test Advantages: - quick to perform - lest expensive - can be standardized - large scale screening - good experiment control - good excellence for mechanism of interaction Disadvantages : relevance to in vivo is questionable
In vivo test : Advantages: - allows complex systemic interaction - response more comprehensive - more relevant Disadvantages: - relevance to use of materials questionable - time consuming - legal / ethical concerns - difficult to control - difficult to interpret and quantity
Usage test Advantages : - relevance to use of material is assured Disadvantages: - very expensive - very time consuming - major legal/ethical issue - can be difficult to control - difficult to interpret and quantity
ANSI / ADA Specification 41 3 category of test (1982): - initial test - secondary test - usage test : a. placement of the materials in intended b. first in larger animal / primates c. Food & drug Administration approval ISO 10993 - ISO 10993 ( 1992) - ISO 7405 (1997) revised
The vast advance of cellular & molecular biology The variety of test available for assessing biocompatibility of material The lack of standardization of these test
Initials Tests - Short term systemic toxicity test: Oral route - Acute systemic toxicity test: Intravenous route - Inhalation toxicity test - Hemolysis test - Ames mutagenicity test - Styles cell transformation test - Dominant lethal test - In vitro cytotoxicity test (Cr release) - Cytotoxicity test (Millipore filter) - Tissue culture agar overlay test
Secondary Tests - Subcutaneous implant test - Bone Implant - Sensitization test - Oral mucous membrane irritation test Usage Test - Oral mucous membrane irritation test - Pulp and dentin test - Pulp capping and pulpotomy test - Endodontic usage test - Bone implant usage test
Penetapan toksisitas material jangka pendek Hewan coban: 40 tikus, 8 minggu, 130-150 mg BB Kandang: 33 x 28 x 16 cm, 5 tikus, diet standart Material dibuat serbuk larutan/suspensi atau dicampur dlm makanan (dosis 1 g/kg BB) Cara pemberian materi: dgn alat intragastric needle, atau stomach tube (kontrol dgn aquadest) Observasi: 7 hari, amati perub. dan timbang BB/hr Euthanasia dgn eter (inhalasi) kmd necropsy Interprestasi: mati, toksik klinik, BB, jaringan
Hewan coba, perkandangan spt STSTT oral Materi: dilarutan dlm 0,9% NaCl, Cara pemberian: suntikan i.v pada vena cauda dgn dosis 5 ml/100 g BB, bila tak larut extract 4 g dipotong kecil-kecil, masukkan dlm 20 ml saline normal, di autoclve 121o C 1 jam, semua extrac disuntikkan Pengamatan: observasi selama 7 hari Euthanasia dgn eter dan necropsy Interprestasi: mati, toksik klinik, BB, jaringan
Hemolysis Test
Evaluasi aktivitas hemolitik pada bahan yang kontak lama Rational: - hemolitik dasar: pelepasan Hb - hemolitik komponen solubel dan permukaan fisik: total hemoltik Material: centrifuge, waterbath, test tube, spectro-fotometer, tabung pipa darah Prosedur: - Darah kelinci oksalat : 0,2 ml di hemilisis dalam 10 ml akuades (dibaca pada : 545 nm : 0,8 0,5 o.d)
- Bahan 5 gr (dipotong 0,5 mm) dlm 10 ml saline normal dlm waterbath 37oC selam 30 menit - Kontrol + : 0,2 ml lar. darah dlm 10 ml akuades - Kontrol - : 0,2 ml lar. darah dlm 10 ml saline normal (o.d < 0,3) (o.d sampel o.d kontrol neg) % hemolisis = ------------------------------------ x100% (o.d kontrol pos - o.d kontrol neg) Uji antar mean statistik Respon hemolisis > respon kultur jaringan
Hewan coba: tikus Rational: Prosedur: - implan 3 mm () x 10 mm (p) - insisi 0,5 cm kemudian diseksi tumpul + I cm - evaluasi pada 48 jam, 2 minggu dan 12 minggu. (inflamasi, nekrosis, pertinent changes) - Kriteria : tidak ada reaksi inflamasi / reaksi ringan, moderat, parah
Ketentuan implan - Bahan diterima : a. tdk ada/reaksi ringan pd minggu 2 dan 12 b. reaksi moderat pd minggu ke hilang pada 12 - Bahan ditolak: a. ada reaksi ringan pd minggu ke 2 meningkat ke moderat/ parah pada ke 12 b. Reaksi moderat pada minggu 2 dan 12 c. Reaksi parah pada minggu 2 dan 12
Reaction of pulp Microleakage: .. (nanoleakage) - contracting during polymerization - wear - thermal cycling saliva invasion microorganism inflammation/infection
Dental bonding - bonding to dentin has proven more difficult a. organic and inorganic b. wettability >> EDTA, Na-hypochloride c. lower mineral content (in dentin) - occurred hybrid layer of resin & collagen - removal of smear layer caused: a. its juxtaposes resin & dentin without barrier b. make any microleakage more significant c. acid are potential source irritation
Dentin bonding agent cytotoxicity: HEMA 100 X less toxic than bis-GMA - combination HEMA and other resin, act synergis tically - some resin component enhance the growth of oral bacteria - the ability of resin based material to increase plaque formation
Resin base materials release (Resin composite: organic & inorganic phase) - freshly set chemically & light cured resin cause moderate cytotoxicity, and reduced 24-72 hours (with dentin barrier) - be mediated by resin component release - light cure < chemically cure (depend on : efficiency of the light and type of resin) - reaction diminished 5 8 weeks and an increase in reparative dentin
Latex - 6-7% surgical personnel may be allergic to latex - 42% dental personnel: dermatoses of hands & finger - hypersensitivity reaction was cause by true latex, accelerator or antioxidant (in processing) Nickel - the most allergenic metal (10-20%) - is a known cross-reactivity between Ni and Pd patient who are allergic Ni will be allergic to Pd - Ni sulfide is a respiratory carcinogen - Ni+ is a mutagenic in human
Beryllium - Beo & Be + is a carcinogenic - acidic environment enhance Be release from Ni-Cr - Be - containing particle (dust) that are inhaled cause berylliosis
Mercury - access to the body via the skin or vapor - toxic effect is 3 g/kg
Estrogenicity - bisphenol A (BPA & BPAD) is a estrogenic effect - evidence comes from estrogen receptor-BPA binding Residual Resin - to be allergy because exposure to unpolymerized materials. - have significant toxic effect (invitro test) - the use of glove is not effective in preventing to monomer resins - resin component have been to transverse the dentin
Amalgam: - by corrosion product release (2) - marginal microleakage - mercury residu Glass ionomer - freshly prepared is mildly cytotoxixity - fluoride release (cytotoxicity in vitro) - increased dentin permeability after etching
Liners, Varnishes & non resin cement Liners (CaOH) : - pH alkaline (12) extreem cytotoxicity - containing resin mild to moderate in culture varnish containing copal & polystyrene - resin component dissolve - formation pinpoint holes Non resin ZnPO4 : low pH and leaching of Zn Zn OE : suppresses nerve transmission and anti inflammatory Bleach agent - peroxide can rapidly traverse the dentin - chemically burn the gingiva
- product of bacterial plaque & accumulate - buffering & protein-bonding to mitigate cytotoxic - direct contact resin composite with fibroblast caused leach out un polymerized component - roughness surface - hypersensitivity of the acrylic & diacrylic monomers
(osseointegration / biointegration)
Van der Waals force Mechanical entrapment Compressive force Chemically bond
Bioactive - Ceramic
TISSUE
BIOGLASS Na O - Si Si O Si
Cation & silica Dissolution network Silanol formation Silica gel forms by condensation of silanols (silane chain) Calcium-phosphate-rich mineral forms
H OH
H O Si Si O Si Si O Si O O
Ca & PO4
Ca10(PO4)6(OH)F
Diffusion oxygen and metals ion into tissue Diffusion hydrogen and oxygen into tissue to form hydroxides Diffusion of mineral or atoms from electrolyte in to the oxides Dissolution of oxide metal ion (corrosion) Adsorption at biomolecular Desorption for replacement of biomolecular Fragmentation of modification of biomolecular