ライフサイエンスコーパス: LCST

1 LCST events triggered by the addition of a kosmotropic s

2 e pendant acid or basic group and undergo an LCST event, the LCST event can change the bulk solution

3 ogically active peptide repeats that exhibit LCST or UCST transitions.

4 ize, with larger particles exhibiting higher LCST values.

5 olvent isotope effects and of the changes in LCST with ion concentration and identity showed multiple

6 rse thermal stimulation to below the PNIPAAm LCST, the beads and captured streptavidin were observed

7 The PIL's LCST-type transition temperature can also be influenced

8 okes radius measurements below the polymer's LCST using gel filtration chromatography.

9 rings to light the presence of a second, sub-LCST transition, observed well below the LCST of oligo(e

10 This sub-LCST transition is accompanied by changes in the guest e

11 ower or upper critical solution temperature (LCST and UCST, respectively) transitions in physiologica

12 have a lower critical solution temperature (LCST) above physiologic temperature, such that the mater

13 ove its lower critical solution temperature (LCST) and its release and bioactivity was measured.

14 -called lower critical solution temperature (LCST) behavior has been well-studied, there have been no

15 with a lower critical solution temperature (LCST) in the range of ~25-35 degrees C.

16 The lower critical solution temperature (LCST) of elastin-like polypeptides (ELPs) was investigat

17 eds the lower critical solution temperature (LCST) of PNIPAAM, micelle solutions (at >/=2.5 wt %) sha

18 ove the lower critical solution temperature (LCST) of PNIPAAm, the beads aggregate and adhere to the

19 hat the lower critical solution temperature (LCST) of PNIPAM decreased as urea was added to the solut

20 ove the lower critical solution temperature (LCST) of PNIPAM.

21 on the lower critical solution temperature (LCST) of poly(N-isopropylacrylamide), PNIPAM, was invest

22 ove the lower critical solution temperature (LCST) of the polymer (approximately 30 degrees C).

23 ond the lower critical solution temperature (LCST) of the polymers used.

24 exhibit lower critical solution temperature (LCST) phase transition behavior, can exist in a coupled

25 of the lower critical solution temperature (LCST) phase transition of individual hydrogel particles

26 ersible lower critical solution temperature (LCST) phase transition.

27 at have lower-critical solution temperature (LCST) properties experience a water-like environment bel

28 to the lower critical solution temperature (LCST) properties of Pluronic F127, the particles exhibit

29 radable lower critical solution temperature (LCST) segments are applied to prepare such dynamic aggre

30 ophobic lower critical solution temperature (LCST) transition exhibited by a recombinant, stimuli-res

31 CST) or lower critical solution temperature (LCST) type of phase behavior as novel thermolytic osmoti

32 ponsive lower critical solution temperature (LCST) were created through the copolymerization of an am

33 ove the lower critical solution temperature (LCST), PNIPAAm provides a liphophilic microenvironment w

34 low the lower critical solution temperature (LCST), resulting in a tunable release rate of the drugs

35 ibits a lower critical solution temperature (LCST)-type thermal responsive behavior.

36 ove its lower critical solution temperature (LCST).

37 pendent lower critical solution temperature (LCST).

38 on at a lower critical solution temperature (LCST).

39 The LCST phase transition originates from the interaction be

40 The LCST transition of the grafted ELP and the ELP fusion pr

41 The LCST transition results in capture of the ELP fusion pro

42 The LCST-induced dethreading of the polymer-based pseudorota

43 ng Trx-ELP/anti-Trx complex formed above the LCST could be reversibly dissociated below the LCST.

44 r is soluble but are less hydrated above the LCST when the polymer phase separates from solution.

45 n protein onto the ELP nanopattern above the LCST.

46 es and areas of vibrational bands across the LCST transition for PNIPAM whereas NIPAM exhibits a cont

47 yl acrylamide (NIPAM) in solution across the LCST transition.

48 tic strategy of this bioconjugate allows the LCST of the material to be changed readily from a common

49 sub-LCST transition, observed well below the LCST of oligo(ethylene glycol) (OEG)-based dendrons, whe

50 xperience a water-like environment below the LCST where the polymer is soluble but are less hydrated

51 curring at the electrode above and below the LCST.

52 ST could be reversibly dissociated below the LCST.

53 that these substituted compounds caused the LCST of PNIPAM to rise with increasing methyl group cont

54 r basic group and undergo an LCST event, the LCST event can change the bulk solution pH.

55 found that there is a greater change in the LCST value between H(2)O and D(2)O for those polypeptide

56 Differences in the LCST values with heavy and light water were correlated w

57 ata which indicated that the decrease in the LCST was coupled to the direct hydrogen bonding of urea

58 e ability of a particular anion to lower the LCST generally followed the Hofmeister series, analysis

59 tion-triggered, allosteric regulation of the LCST phase transition of a polymer and are significant b

60 se they expand the available triggers of the LCST transition of stimulus-responsive polymers to bioch

61 lymer thermodiffusion in the vicinity of the LCST.

62 s released from the surface by reversing the LCST transition.

63 For coupled hydration shells, the LCST phase transition characterized by spin probing cont

64 ermore, NIR-MSI measurements reveal that the LCST value is unique for each individual hydrogel partic

65 The ability to allosterically trigger the LCST transition of ELPs by biomolecular recognition will

66 xy group provided a handle through which the LCST was adjusted through small-molecule quenching.