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CROSSLINKS. GELS STRUCTURE. LIQUID PHASE. POLYMERIC CHAINS. MATRICES ARE COHERENT SYSTEMS MADE UP BY A POLYMERIC NETWORK TRAPPING A CONTINUOUS LIQUID PHASE. THEY SHOW MECHANICAL PROPERTIES IN BETWEEN THOSE OF SOLIDS AND LIQUIDS. 20 m m. 0.2 m m.
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CROSSLINKS GELS STRUCTURE LIQUID PHASE POLYMERIC CHAINS MATRICES ARE COHERENT SYSTEMS MADE UP BY A POLYMERIC NETWORK TRAPPING A CONTINUOUS LIQUIDPHASE. THEY SHOW MECHANICAL PROPERTIES IN BETWEEN THOSE OF SOLIDS AND LIQUIDS
20 mm 0.2 mm Schneider et al. J. American Chemical Society, 2002. (a) Laser scanning confocal microscopy. Green regions are fluorescently stained self-assembled peptide, and black regions are water-filled pores and channels. (b) CryoTEM. Dark structures are selfassembled peptide scaffold, while lighter gray areas are composed of vitrified water.
PHYSICAL CROSSLINKS (weak) ENTANGLEMENTS (TOPOLOGICAL CONSTRAINS) CONNECTING DISORDERED ZONES Van der Walls, dipole-dipole, hydrogen bonding, Coulombic hydrophobic interactions ORDERED ZONES POLYSACCARIDES (GLUCANS, XANTHAN)
PHYSICAL CROSSLINKS (strong) Ca++ Ca++ Ca++ Ca++ Ca++ Ca++ Ca++ EGGS BOX STRUCTURE INTERACTION BETWEEN THE BIVALENT ION AND GULURONIC UNIT ALGINATES
CHEMICAL CROSSLINKS (strong: covalent bond) SCLEROGLUCAN CROSSLINKED WITH BORAX T. Coviello et al., Int. J. Biol. Macromolecules, 32 (2003) 83
POROUS GELS: Cellulose – Acrylic Acid Crosslinking irradiation intensity Cellulose mass fraction Acrylic acid mass fraction
a) Monomer dilution e) Oxidant b) Neutralization f) Reductant c) Crosslinker g) Bicarbonate d) Foaming aid and stabilizer SPH a) Monomer dilution e) Oxidant thermal initiator b) Neutralization f) Reductant c) Crosslinker d) Foaming aid g) Bicarbonate SAP Figure 6.2. Schematic representation of steps involved in the production of Super porous hydrogels (SPH) and Super absorbent polymers (SPA) (with permission from ref.[46]).
POROSITA’ 2*RD RP FARMACO CATENE POLIMERICHE RD/RP 0.01 0.1 MEZZO CONTINUO MEZZO POROSO Il moto del farmaco avviene tra le maglie del reticolo polimerico contenenti anche le molecole del fluido di rilascio Il moto del farmaco avviene nel fluido di rilascio che riempe i canali le cui pareti sono costituite dal polimero ZONA INTERMEDIA
DIFFUSIONE R = 0 DRUG R = Rp TORTUOSITA’ Lc/Rp POROSITA’ Vv/VT De=Dw*e/t
IMPRINTED GELS I I I COMPLEX FORMATION I I CROSSLINKING I I = initiator WASHING = template = functional monomers = crosslinking monomers MOLECULAR IMPRINTING
IMPRINTED POLYMERIC GELS: CHARACTERISTICS Binding affinity: a measure of how well the template molecule is attracted to the binding site Selectivity : the ability to differentiate between the template and other molecules Binding capacity : the maximum amount of template bound per mass or volume of polymer
BINDING AFFINITY Forward reaction (binding) Backward reaction (un-binding) Association constant Macromolecular sites concentration Template concentration
SELECTIVITY a = Ka1/Ka2 1 ≤ a≤ 8
A A A A A A A A A A A A A A A A A A A A A P P P P P P P P P A A A A = PROTEIN = DRUG NETWORK SWELLING: DRUG CAN BE RELEASED A =ANALYTE EXAMPLE : SWELLING CONTROL
EXAMPLE 2: TARGETED DELIVERY TISSUES OR CELLULAR LINING HYDROGEL DRUG CELLULAR RECEPTOR IMPRINTED FILM R R
BIBLIOGRAFIA • Lapasin R, Pricl S, Rheology of Industrial Polysaccharides; Theory and Applications, Chapman and Hall, London, 1995. • Coviello T, Grassi M, Rambone G, Santucci E, a Carafa M , Murtas E, Riccieri F M, Franco Alhaique F. Novel hydrogel system from scleroglucan: synthesis and characterization J. Contr. Rel. 60, 367–378, 1999. • A. Kydonieus (Ed.), Treatise on Controlled Drug Delivery, Marcel Dekker, New York, 1992, pp. 54-55. • Colombo, P. 1993. Swelling-controlled release in hydrogel matrices for oral route. Adv. Drug. Dev. Rev., 11, 37 – 57 • Grassi M, Colombo I, Lapasin R. Drug release from an ensemble of swellablecrosslinked polymer particles. J. Contr. Rel. 68, 97-113, 2000.