• Applied Chemistry for Engineering
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• v.10 no.3
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• pp.445-449
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• 1999

Hydrophilic polyphosphazenes were synthesized from hydrophobic polyphosphazenes by adding methoxyethylenoxy side chains and cast by dip-coating method into membranes supported on porous polypropylene mesh filter sheet for metal separation testing. A solution of $Cr^{3+},\;Co^{2+},\;Mn^{2+}$ nitrates was used in diffusion experiments which were conducted from $25^{\circ}C$ to $60^{\circ}C$. lt was found that the ion transport properties were increased as the repeating number of ethylenoxy side chain increased. Membrane from trifluoroethoxy methoxyethoxyethoxyethoxy co-substituted polyphosphazenes was found to separate $Cr^{3+}$ ion from $Mn^{2-}$ and $Co^{2+}$ ions with separation factor of 4.5 at $60^{\circ}C$.

• Proceedings of the Korean Fiber Society Conference
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• 1991.06b
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• pp.15-16
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• 1991

• Bulletin of the Korean Chemical Society
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• v.22 no.11
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• pp.1243-1247
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• 2001

The water-soluble poly(aminoaryloxy-methylamino phosphazene) has been synthesized and investigated as a polymeric carrier species for the covalent attachment of biologically active agents. The cyclic trimeric model systems were utilized for the synthesis of polymeric analogues containing bioactive side groups. The sodium salt of 4-acetamidophenol was first allowed to react with (NPCl2)3 or (NPCl2)n and was then treated with excess methylamine to yield derivatives of type [NP(NHCH3)x(OArNHCOCH3)y]3 or [NP(NHCH3)x(OArNHCOCH3)y]n. The 4-acetamido groups were then hydrolyzed to 4-aminophenoxy units with potassium tert-butoxide. Coupling reactions between amino group and N-acetylglycine was accomplished with the use of dicyclohexylcarbodiimide. Their properties and structural characterization are discussed.

• Polymer Science and Technology
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• v.8 no.3
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• pp.306-315
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• 1997

• Journal of Pharmaceutical Investigation
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• v.25 no.2
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• pp.109-116
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• 1995

For the administration of narcotic antagonist with short half-life and low patient compliance, the sustained release system using biodegradable matrix is effective. Polyphosphazenes are of considerable interest as biodegradable matrix systems for controlled release of drugs. In this study, biodegradable polyphosphazenes available for the sustained release implantable device were synthesized, and their application was examined. Poly[dichlorophosphazene] was synthesized by solution polymerization method and confirmed with IR spectrum. Poly[bis(ethyl glycinate) phosphazene] and poly[ (diethyl glutamate)-co-(ethyl glycinate)phosphazene] were then produced by substitution of amino acid alkyl esters for chloride side groups. Using these polymers, the implantable devices of 1 mm thickness and $10{\times}10\;mm$ size containing naloxone hydrochloride were prepared and their release and degradation profiles were measured. In the case of poly[bis(ethyl glycinate)phosphazene] with swelling characteristics, degradation rate was slower than the release rate, showing that the release rate is partly dependent on the swelling rate. In contrast, the degradation rate of polyl[(diethyl glutamate)-co-(ethyl glycinate)phosphazene] matrix was identical with release rate of naloxone hydrochloride. On the basis of these results, it is expected that these polymers can be applied to sustained release implantable systems delivering narcotic antagonist.

• Bulletin of the Korean Chemical Society
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• v.16 no.11
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• pp.1074-1079
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• 1995

Poly(dichlorophosphazene) having low molecular weight (M&bar;w∼104) was synthesized by the thermal reaction of hexachlorocyclotriphosphazene in the presence of excess AlCl3 (>2%) as catalyst. Using the poly(dichlorophosphazene), poly[bis(ethylglycino)phosphazene], poly[bis(glycinemethylamido)phosphazene], and poly[(glycinemethylamido)(methylamino)phosphazene] were prepared. Diammineplatinum(Ⅱ) complex cation was introduced into these derivatized phosphazene polymers, and the resultant polymers containing the platinum(Ⅱ) moiety were charaterized by means of elemental analysis, IR and NMR spectroscopies, and then subjected to in vitro and in vivo assays of antitumor activity.

• Membrane Journal
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• v.27 no.2
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• pp.138-146
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• 2017

The new types of phenoxy-carboxylatophenoxy cosubstituted polyphosphazene were synthesized with various substitution rates. Diabetic diagnostic membranes were prepapared with these types of polyphosphazenes and final absorbances at 680 nm through these membranes were measured at various concentrations of glucose in blood. Basically, the end-point results of varying absorbance values according to time (K/S) had a linear relationship to the glucose concentration. The effects of substitution rates with hydrophilic carboxylatophenoxy groups and hydrophobic phenoxy groups on the glucose concentration measurements were examined. It was very difficult to measure glucose concentration in less than 10% of the hydrophilic substitution rates, because the glucose penetration rate was too slow. But dose-response slope (DRS) values between glucose concentration and K/S values increased as the hydrophilic substitution rates increased in more than 10% of the hydrophilic substitution rates. However, in more than 30% of the hydrophilic substitution rates, DRS value was too rapidly increased, because glucose penetration rate was too fast.

• Proceedings of the Membrane Society of Korea Conference
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• 1998.10a
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• pp.123-126
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• 1998

1960년 Allcock이 공기중에서 안정한 포스파젠고분자를 합성한 이래 포스파젠고분자는 열적, 화학적 안정성, 그리고 -P=N-골격에 다양한 측쇄를 부착함으로써 화학적으로 쉽게 고분자를 변형시킬 수 있다는 특징으로 인하여 이온교환막을 위한 기본고분자로 많은 관심을 끌고 있다. 1986년 MaCaffery등은 trifluoro- ethoxy를 치환한 고분자막을 합성하여 고온 안정성에 대한 특성을 실험한 바 있으며 1989년 Allen과 Macffrey등은 bistrifluoroethoxy를 치환시킨 포스파젠고분자를 합성하여 Co와 Mn이 들어있는 용액으로부터 Cr을 분리하였다. 그러나 trifluoroethoxy가 치환된 막은 소수성의 특징을 보이기 때문에 친수성이 요하는 곳에의 응용에는 사용할 수가 없었다. 친수성 포스파젠고분자의 합성의 경우는 1988년 Allcock과 Kwon등이 방사선을 이용하여 가교결합시켜 물에 녹지 않는 포스파젠 친수성 겔을 합성한 바 있으며 1990년 Wycisk등은 포스파젠 고분자를 슬폰화시켜 친수성을 가진 이온교환막을 합성하였다.

• Bulletin of the Korean Chemical Society
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• v.21 no.10
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• pp.1039-1040
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• 2000

The water-soluble poly(methoxyethoxy-aminoarlyoxy phosphazene) has been synthesized and investigated as a polymeric carrier molecule for the covalent attachment of bioactive agents. The synthetic procedures were developed first through the use of cyclic trimeric model systems. These model systems were utilized for the synthesis of polymeric analogues containing bioactive side groups. The sodium salts of 2-methoxyethanol and 4-acetamidophenol were allowed to react with $(NPCl_2)_3$ or $(NPCl_2)n$ or to yield derivatives of type $[NP-(OCl_2CH_2CH_2OCH_3){\chi}(OArNHCOCH_3)y]_3or$ n. The 4-acetamido groups were then hydrolyzed to 4-amino-phenoxy units with potassium tert-butoxide. Coupling reactions between amino group and N-acetylglycine was accomplished with the use of dicyclohexylcarbodiimide. Their properties and structural characterization are discussed.

• Membrane Journal
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• v.23 no.4
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• pp.297-303
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• 2013

Diagnostic membranes which were made of polyphosphazenes were prepared for the measurements of blood glucose concentration. The effects of possible interferents in human blood on the glucose concentration measurements were examined. Above those interferents, ascorbic acid (AA) showed 3~9% higher K/S values compared to the standard plasma solution, tolbutamide (TA) showed 11~13% lower K/S values than those of plasma, triglycerides and bovine serum albumin (BSA) showed 20~25% lower K/S values than those of plasma. However, most of the interferents except above materials did not show any serious effects on the blood glucose measurements.