ライフサイエンスコーパス: polyvinyl alcohol

1 paints, polyvinyl chloride, polystyrene and polyvinyl alcohol.

2 e-templating strategy with the assistance of polyvinyl alcohol.

3 ccurs in the absence of crowding agents like polyvinyl alcohol.

4 ly, we reported the synthesis of amphiphilic polyvinyl alcohol and dextrin-based nanogel conjugates w

5 ved using polyelectrolyte hydrogels based on polyvinyl alcohol and polyacrylic acid.

6 ffinose, and dextran 5000), linear polymers (polyvinyl alcohol and polyvinyl pyrrolidone) or guanidin

7 ne as a precursor of the inorganic phase and polyvinyl alcohol as the organic component, and incorpor

8 s constructed by entrapment of the enzyme in Polyvinyl Alcohol (azid unit) on Cobalt-Phtalocyanine (C

9 Polyvinyl alcohol-based reservoir implants releasing EMD

10 ons of soluble protein or by implantation of polyvinyl alcohol devices containing protein.

11 asic pigmentation response was obtained when polyvinyl alcohol film containing lysine was treated wit

12 ly 54, 760 cm-1 M-1, f approximately 1.1) in polyvinyl alcohol films are studied.

13 atics via infrared fluorescent emission, and polyvinyl-alcohol functionalized SWCNTs that act as an i

14 ling lipid precursor films on top of a dried polyvinyl alcohol gel surface in a swelling buffer that

15 g poly(lactic-co-glycolic acid) microspheres/polyvinyl alcohol hydrogel composite coatings were adapt

16 ly(lactic-co-glycolic acid) microsphere/PVA (polyvinyl alcohol) hydrogel composite coatings have been

17 in and mercuric chloride-based low-viscosity polyvinyl alcohol (LV-PVA) are widely used by most diagn

18 re carried out in isolated murine epidermis, polyvinyl alcohol/lysine films, and lysine in glycerol/w

19 acteriorhodopsin molecules are embedded in a polyvinyl alcohol matrix has been investigated by using

20 of this method can be enhanced by combining polyvinyl alcohol-mediated growth with inverse-phase met

21 Incorporation of two vinyl polymers, polyvinyl alcohol (molecular weight, 50,000) (PVA-50) an

22 tcomes with the use of nonspherical particle polyvinyl alcohol (nsPVA).

23 ucus, whereas PLGA nanoparticles coated with polyvinyl alcohol or Vitamin E conjugated to 1 kDa PEG w

24 0.1% fluorometholone (FML group) or topical polyvinyl alcohol (PA group) for 22 days.

25 an, 100-mum) and 180-300-mum (mean, 200-mum) polyvinyl alcohol particles was performed by means of a

26 was significantly higher in the fibrin glue, polyvinyl alcohol particles with coils, and n-butyl cyan

27 saline (sham), gelatin sponge, fibrin glue, polyvinyl alcohol particles with coils, n-butyl cyanoacr

28 Polylactic acid microspheres, polyvinyl alcohol particles, and absorbable gelatin powd

29 TAE with 1 mg (group 1) or 3 mg (group 2) of polyvinyl alcohol particles.

30 irabile was embolized with PAN microbeads or polyvinyl alcohol particles.

31 ght pigs by using a combination of coils and polyvinyl alcohol particles.

32 rmed using stool that is chemically fixed in polyvinyl alcohol (PVA) and formalin, after which the st

33 -co-glyclic acids (PLGA) and emulsified in a polyvinyl alcohol (PVA) and NaCl solution of small volum

34 idase (GOD) in a composite material based on polyvinyl alcohol (PVA) and partially prehydrolyzed tetr

35 Herein, we validated polyvinyl alcohol (PVA) as a single-molecule environment

36 Polyvinyl alcohol (PVA) containing the fixative mercuric

37 Depending on the thickness of the polyvinyl alcohol (PVA) film on the silver, the coupling

38 hermal decomposition and chemical changes of polyvinyl alcohol (PVA) in a titania (TiO(2)) matrix and

39 ative (STF) as a substitute for formalin and polyvinyl alcohol (PVA) in fecal preservation.

40 Dye-loaded nanocapsules are immobilized in a polyvinyl alcohol (PVA) matrix with high solvent permeab

41 trated specimens preserved in either mercury-polyvinyl alcohol (PVA) or cupric PVA.

42 noids, we transplanted 800 mouse islets into polyvinyl alcohol (PVA) or polyglycolic acid (PGA) polym

43 is group, 25 women were treated with Contour polyvinyl alcohol (PVA) particles, 23 were treated with

44 cisional wounds and subcutaneously implanted polyvinyl alcohol (PVA) sponges were analyzed.

45 from mercuric chloride-based Schaudinn's and polyvinyl alcohol (PVA) stool preservatives to other, no

46 alysis revealed a thin discontinuous film of polyvinyl alcohol (PVA) surfactant (circa 4.5 nm thick)

47 estigate the influence of surface coating by polyvinyl alcohol (PVA), a relatively hydrophilic and un

48 ar scaffolds, bovine serum albumin (BSA) and polyvinyl alcohol (PVA), as chemically complementary pla

49 ter linkage to a common hydrophilic polymer, polyvinyl alcohol (PVA), creating an amphiphilic nanomat

50 n, conventional high MW emulsifiers, such as polyvinyl alcohol (PVA), interrupts the PEG coating on n

51 cient method of introducing radiopacity into Polyvinyl alcohol (PVA)-2-Acrylamido-2-methylpropane sul

52 be (MWCNT) enhanced composite electrodes and polyvinyl alcohol (PVA)-poly (acrylic acid) (PAA) copoly

53 n a three-electrode cell) or 300 F cm(-3) in polyvinyl alcohol (PVA)/H(3)PO(4) electrolyte (measured

54 E) immobilized in a azide-unit water-pendant polyvinyl alcohol (PVA-AWP)/Fe-Ni alloy nanocomposite.

55 lary muscles can be achieved by injection of polyvinyl-alcohol (PVA) polymer, a biologically inert bi

56 20%) and concentration of stabilizing agent (polyvinyl alcohol, PVA: 1-3%).

57 A polyvinyl alcohol solution was applied to array surfaces

58 o an inflammatory stimulus (ie, subcutaneous polyvinyl alcohol sponge implantation) was markedly dimi

59 otype by neutrophils was studied in the s.c. polyvinyl alcohol sponge wound model in mice made neutro

60 iltrating leukocytes into Matrigel plugs and polyvinyl alcohol sponges containing conditioned media d

61 WF were isolated from polyvinyl alcohol sponges implanted in male Lewis rats a

62 observed in m isolated from PGE(2)-enriched polyvinyl alcohol sponges implanted in murine wounds.

63 We implanted polyvinyl alcohol sponges subcutaneously in the dorsa of

64 e were subjected to a midline laparotomy and polyvinyl alcohol sponges were implanted subcutaneously

65 Polyvinyl alcohol sponges were implanted to elicit a nai

66 on with subcutaneous implantation of sterile polyvinyl alcohol sponges, or to 1.5 x 1.5-cm dorsal ski

67 rotic tissue within subcutaneously implanted polyvinyl alcohol sponges.

68 rostatic hyperplasia with spherical particle polyvinyl alcohol (sPVA) and compare outcomes with the u