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1 e response compared with poly(lactic acid-co-glycolic acid).
2 ive poly-beta amino ester and poly lactic-co-glycolic acid.
3 lymerisation reactions using amino acids and glycolic acid.
4 cord of clinical translation, poly(lactic-co-glycolic) acid.
5 ant, and plasticizer solvents, polylactic-co-glycolic acid (30% by solids volume), and regolith simul
6 SNAP) was encapsulated within poly(lactic-co-glycolic acid) 50:50 (PLGA) microspheres by using a soli
7 -based ILs (1 week); (2) bare poly(lactic-co-glycolic acid) (50:50, acid terminated) Resomer 504H (PL
9 When biodegradable polymers poly(lactic-co-glycolic) acid and polylactic acid were included in the
10 we present a novel polymer of poly(lactic-co-glycolic) acid and polyvinyl alcohol that can serve as a
11 system containing a blend of poly(lactic-co-glycolic acid) and a representative poly(beta-amino) est
12 cles that perform better than poly(lactic-co-glycolic acid) and iron oxide, two commonly studied mate
13 odegradable polymers such as poly (lactic-co-glycolic acid) and polycaprolactone have been used to fo
14 tion of diblock copolymers of poly(lactic-co-glycolic acid) and polyethylene glycol (PLGA-PEG) using
15 o 50% (w/w) sirolimus drug in poly(lactic-co-glycolic acid) and were prepared on both MP35N metal all
16 fluorescently labeled silica, poly(lactic-co-glycolic acid), and polystyrene nanoparticles administer
17 to undergo rapid oxidation to form glyoxal, glycolic acid, and glyoxylic acid, but the formation of
18 icated by emulsification with poly(lactic-co-glycolic acid) as a core material and, in some cases, po
19 poly(ethylene glycol); PLGA = poly(lactic-co-glycolic acid)) assembled from small AuNRs (dimension: a
20 of aptamer (Apt)-targeted poly(D,L-lactic-co-glycolic acid)-b-poly(ethylene glycol) (PLGA-b-PEG) nano
21 of thermosensitive hydrogels (poly(lactic-co-glycolic acid)-b-poly(ethylene glycol)-b-poly(lactic-co-
22 d using biodegradable diblock poly(lactic-co-glycolic acid)-b-polyethyleneglycol and poly(lactic-co-g
23 cid)-b-polyethyleneglycol and poly(lactic-co-glycolic acid)-b-polyethyleneglycol collagen IV-targeted
25 evant parameters, we report a poly(lactic-co-glycolic acid) based curcumin nanoparticle formulation (
26 acids liberated by the biodegradable lactic/glycolic acid-based polyester, we coincorporated into th
27 f streptavidin-functionalized poly(lactic-co-glycolic acid) beads with biotinylated bovine serum albu
28 cs by blending a targeted poly(d,l-lactic-co-glycolic acid)-block (PLGA-b)-poly(ethylene glycol) (PEG
29 patible and biodegradable poly(D,L-lactic-co-glycolic acid)-block-poly(ethylene glycol) (PLGA-b-PEG)
30 r and carboxyl-terminated poly(D,L-lactic-co-glycolic acid)-block-poly(ethylene glycol) copolymer in
31 lubilization of EpoB in a poly(d,l-lactic-co-glycolic acid)-block-poly(ethylene glycol)-block-poly(d,
33 (PEG-b-PLA) micelles and poly(D,L-lactic-co-glycolic acid)-block-polyethylene glycol)-block-poly(D,L
34 e (NP) based on biodegradable poly(lactic-co-glycolic acid)-block-polyethyleneglycol functionalized w
35 carboxyl functionalization of poly(lactic-co-glycolic acid) can achieve great material homogeneity in
36 tains a core of biodegradable poly(lactic-co-glycolic acid), cholesteryl oleate, and a phospholipid b
37 a moldable alloplastic graft, Poly Lactic-Co-Glycolic Acid-Coated B-Tricalcium Phosphate (PLGA-B-TCP)
38 a moldable alloplastic graft, Poly Lactic-Co-Glycolic Acid-Coated beta-Tricalcium Phosphate (PLGA-bet
39 nd atactic repeating sequence poly(lactic-co-glycolic acid) copolymers (RSC PLGAs) were prepared and
40 ethylene glycol)-block-poly(lactic acid)-co-(glycolic acid) copolymers underwent macroscopic phase se
41 ne provide access to fully substituted alpha-glycolic acid derivatives bearing a beta-stereocenter.
43 r 7-loaded galactosylated poly(DL-lactide-co-glycolic acid) (FGF7-GAL-PLGA) particles; 26-um diameter
44 were created by coating PLGA (poly[lactic-co-glycolic acid]) films containing test compounds with pHE
45 mpare favourably with current poly-lactic-co-glycolic acid fixation systems, however, silk-based devi
46 rous silica nanoparticles and poly(lactic-co-glycolic acid) for the delivery and controlled release o
47 of this study was to evaluate the effects of glycolic acid (GA) (with pH 1.2 and 5) and ethylenediami
48 acid, glycolaldehyde, glyoxal, acetic acid, glycolic acid, glyceraldehyde, 2-hydroxypropanedialdehyd
50 esulted in the selective formation of lactic/glycolic acid glycosides, thereby retaining unique infor
51 ocompatible polymers, such as polylactic and glycolic acid, in order to form stable nanoparticles abl
53 nto valuable C2, C3, and C4 products such as glycolic acid, lactic acid, 2-hydroxy-3-butenoic acid, 2
54 nd dicarboxylic acids (HOOC-R-COOH), such as glycolic acid, lactic acid, glyceric acid, oxalic acid,
55 depot of low molecular weight poly(lactic-co-glycolic) acid (LWPLGA) for sustained delivery GLP-1 and
56 ly(L-lactic acid) and had poly(D,L-lactic-co-glycolic acid) membranes of different molecular masses c
57 ol) dissolution, the flexible poly(lactic-co-glycolic acid) mesh conforms to the resected tumour cavi
58 he form of a micrometre-sized poly(lactic-co-glycolic acid) mesh laid over a water-soluble poly(vinyl
59 rapid prime-boost protocol of poly(lactic-co-glycolic) acid microparticles and a replication-defectiv
61 Apelin-13 encapsulated in poly(lactic-co-glycolic acid) microparticles displayed a sustained rele
63 Dexamethasone-releasing PLGA poly(lactic-co-glycolic acid) microsphere/PVA (polyvinyl alcohol) hydro
65 contraception by formulating poly(lactic-co-glycolic acid) MNs to slowly release the contraceptive h
66 at substitution of the 5'-sulfate in 1 for a glycolic acid moiety in 2 maintains kinesin inhibition.
67 ng a quaternary stereocenter and a protected glycolic acid moiety, which are useful building blocks f
68 prepared from the bioassimilable lactic and glycolic acid monomers for biomedical applications makes
69 rating peptide (CPP)-assisted poly(lactic-co-glycolic acid nanoparticles (PLGA NPs), for improving do
70 then engineered lipid-coated poly(lactic-co-glycolic acid) nanoparticles (NPs) with fibrotic kidney-
71 icity, bevacizumab-loaded poly(D,L-lactic-co-glycolic acid) nanoparticles (PLGA NP) were developed an
72 s remote loading method using poly(lactic-co-glycolic acid) nanoparticles (PLGA NPs) to load myelin o
73 ncapsulated in biodegradable poly (lactic-co-glycolic acid) nanoparticles (PLGA-NP), administered by
74 uch as FDA approved pegylated poly(lactic-co-glycolic acid) nanoparticles (PLGA-PEG-NP) has significa
75 mmunotherapy using CpG-coated poly(lactic-co-glycolic acid) nanoparticles containing peanut extract (
76 tion with AQP4201-220-coupled poly(lactic-co-glycolic acid) nanoparticles could both prevent and effe
77 s method, we found that 80 nm poly(lactic-co-glycolic acid) nanoparticles had maximal K(trans) in a T
78 this study, mannose-decorated poly(lactic-co-glycolic acid) nanoparticles loading with R848 (Man-pD-P
80 ted in negatively charged poly(dl-lactide-co-glycolic acid) nanoparticles, is designed to induce glut
81 degradable polylactic acid and polylactic-co-glycolic acid needles, and its application for the conti
82 m polymeric NPs, specifically poly(lactic-co-glycolic acid) NPs loaded with enrofloxacin (PLGA-Enro N
84 e poly(ethylene glycol)-block-poly(lactic-co-glycolic acid) (PEG-PLGA) copolymers have been used succ
85 radable poly(ethylene glycol)-poly(lactic-co-glycolic acid) (PEG-PLGA) microparticles were engineered
86 growth factor (PCL-NGF) and a poly(lactic-co-glycolic acid) pellet containing glutamine (PLGA-GLN) we
88 lactic acid (PLA)/poly (d)(,)(l)(-)lactic-co-glycolic acid (PLGA) (75:25 w/w) or PHB as encapsulants.
89 ting consisted of absorbable poly-lactide-co-glycolic acid (PLGA) and crystalline sirolimus deposited
90 We created coils with a 50:50 poly-dl-lactic glycolic acid (PLGA) coating that released MCP-1 at 3 di
91 boxymethyl chitosan shell and poly lactic-co-glycolic acid (PLGA) core for enhancing localized chemo-
93 self-healing capacity of poly (DL)-lactic-co-glycolic acid (PLGA) microspheres containing glycosamino
94 conjugated on the surface of poly-lactic-co-glycolic acid (PLGA) nanoparticles for the protection of
95 yvitamin D(3) encapsulated in poly lactic-co-glycolic acid (PLGA) nanoparticles loaded in Pluronic F1
96 ery of FDA-approved pegylated poly lactic-co-glycolic acid (PLGA) nanoparticles loaded with anticance
99 situ-forming implant based on polylactic co glycolic acid (PLGA) was chosen in this preclinical stag
101 onor template encapsulated in Poly Lactic-co-Glycolic Acid (PLGA)-based nanoparticles can correct sic
102 ic acid) peptide-modified polylactic acid-co-glycolic acid (PLGA)-Chitosan nanoparticle (CSNP) for in
103 aded polyethylene glycol-poly lactic acid-co-glycolic acid (PLGA-PEG) polymeric nanoparticles (ARV-NP
104 ulating econazole-impregnated poly(lactic-co-glycolic) acid (PLGA) films in poly(hydroxyethyl methacr
105 polymer coating consisting of poly(lactic-co-glycolic) acid (PLGA) microsphere dispersed in poly(viny
106 locally-delivered Scl-Ab via poly(lactic-co-glycolic) acid (PLGA) microspheres (MSs) was compared at
109 micrometer-sized agent-doped poly(lactic-co-glycolic) acid (PLGA) particles by using a single-emulsi
110 and functionalization of poly (D,L-lactic-co-glycolic) acid (PLGA) particles to enhance cell attachme
111 e) into biodegradable polymer poly(lactic-co-glycolic) acid (PLGA) using an electrojetting technique.
112 tible, the US-FDA-approved, poly(l-lactic-co-glycolic) acid (PLGA) was used to engineer nanoparticles
113 4) and TLR7/8 encapsulated in poly(lactic-co-glycolic) acid (PLGA)-based nanoparticles (NPs) induce r
114 eveloped P-selectin-targeted poly (lactic-co-glycolic) acid (PLGA)-poly (ethylene glycol) (PEG)-based
118 (PCL) (core layer), a 50:50 poly (lactic-co-glycolic acid) (PLGA) (sheath layer) and a gelatin (inte
119 at use of carboxyl-terminated poly(lactic-co-glycolic acid) (PLGA) allowed encapsulation of DSP into
121 articulate nanocarriers using poly(lactic-co-glycolic acid) (PLGA) and PLGA-polyethylene glycol (PLGA
122 nal hydrolytically degradable poly(lactic-co-glycolic acid) (PLGA) and reactive oxygen species (ROS)-
123 loaded with 50% w/w TMZ in poly(lactic acid-glycolic acid) (PLGA) and showed reliable release of hig
124 consisting of water-insoluble poly(lactic-co-glycolic acid) (PLGA) and water-soluble polyvinylpyrroli
125 capsulate vaccine antigens in poly(lactic-co-glycolic acid) (PLGA) by simple mixing of preformed acti
127 anoparticles (CSLPHNPs) with poly (lactic-co-glycolic acid) (PLGA) core and lipid layer containing do
128 rospheres consisting of a poly(d,l-lactic-co-glycolic acid) (PLGA) core surrounded by a poly(lactic a
129 oparticles composed of PSA or poly(lactic-co-glycolic acid) (PLGA) diffused at least 3,300-fold slowe
130 aling of aqueous pores in poly(D,L-lactic-co-glycolic acid) (PLGA) drug delivery systems has been ide
131 tration with nanoparticles of poly(lactic-co-glycolic acid) (PLGA) encapsulating short interfering RN
132 rospinning, consists of a poly(D,L-lactic-co-glycolic acid) (PLGA) fiber layer sandwiched between two
137 s of 25% (w/w) sirolimus in a poly(lactic-co-glycolic acid) (PLGA) matrix and is spray-coated onto me
138 ibility of intra-articular poly(DL-lactic-co-glycolic acid) (PLGA) microparticle (MP) formulations in
139 ined release nor-LAAM-loaded poly (lactic-co-glycolic acid) (PLGA) microparticles (MP) using a hydrop
140 as encapsulated in degradable poly(lactic-co-glycolic acid) (PLGA) microparticles embedded in the PVA
141 rically uniform, monodisperse poly(lactic-co-glycolic acid) (PLGA) microparticles in a robust high-th
142 rogels were encapsulated with poly(lactic-co-glycolic acid) (PLGA) microparticles loaded with vascula
143 he scaffolds and accommodated poly(lactic-co-glycolic acid) (PLGA) microparticulate systems that cont
146 eloped Sunb-malate loaded poly(D,L-lactic-co-glycolic acid) (PLGA) microspheres (Sunb-malate MS) with
148 is released for 4 weeks from poly(lactic-co-glycolic acid) (PLGA) microspheres embedded in a poly(N-
149 injectable and biodegradable poly(lactic-co-glycolic acid) (PLGA) microspheres encapsulating a model
150 of long-acting injectables, poly (lactic-co-glycolic acid) (PLGA) microspheres have been extensively
151 and porosity distributions in poly(lactic-co-glycolic acid) (PLGA) microspheres were characterized us
152 microtubes and NEP1-40 into poly (lactic-co-glycolic acid) (PLGA) microspheres, obviating the need f
153 H inside the aqueous pores of poly(lactic-co-glycolic acid) (PLGA) microspheres, often termed microcl
155 icles (LPNs) consisting of poly(DL-lactic-co-glycolic acid) (PLGA) nanocarriers modified with the cat
156 or were entrapped within the poly (lactic-co-glycolic acid) (PLGA) nanoparticle, which was then encap
158 were encapsulated within poly(d,l-lactic-co-glycolic acid) (PLGA) nanoparticles (COUR CNPs) to asses
159 act by encapsulating it into Poly (lactic-co-glycolic acid) (PLGA) nanoparticles (FI-PLGA NPs) and ev
160 as to evaluate the ability of poly(lactic-co-glycolic acid) (PLGA) nanoparticles (NP) to enhance lute
162 tudy, SV7 was encapsulated in poly(lactic-co-glycolic acid) (PLGA) nanoparticles (NPs) to improve the
163 lation of the compound within poly(lactic-co-glycolic acid) (PLGA) nanoparticles (PLGA-EtNBS) was fou
164 y silent reduced state inside poly(lactic-co-glycolic acid) (PLGA) nanoparticles (PTX-MB@PLGA NPs).
165 proteins formulated in poly-(D, L-lactic-co-glycolic acid) (PLGA) nanoparticles adjuvanted with poly
166 ery system for siRNA based on poly(lactic-co-glycolic acid) (PLGA) nanoparticles and combined this sy
168 s, including the widely used poly (lactic-co-glycolic acid) (PLGA) nanoparticles contained in slow-re
170 hibitor 1a,25(OH)(2)D(3) from poly(lactic-co-glycolic acid) (PLGA) nanoparticles embedded in a thermo
171 tential of galantamine-loaded poly(lactic-co-glycolic acid) (PLGA) nanoparticles for SCI treatment.
174 inducing adjuvant based on poly(dl-lactic-co-glycolic acid) (PLGA) nanoparticles modified with the ca
175 the activity of the peptide, poly(lactic-co-glycolic acid) (PLGA) nanoparticles were surface-modifie
176 tation, we have prepared poly(lactic acid-co-glycolic acid) (PLGA) nanoparticles with a PEGylated sur
177 t how surface modification of poly(lactic-co-glycolic acid) (PLGA) nanoparticles with peptide ligand
181 ties, was encapsulated within poly(lactic-co-glycolic acid) (PLGA) NPs (Api-NPs) for localized delive
182 we report the formulation of poly(lactic-co-glycolic acid) (PLGA) NPs by nanoprecipitation and the a
183 ed fluorescent, biodegradable poly(lactic-co-glycolic acid) (PLGA) NPs in a range of sizes (120-440nm
184 he method was demonstrated on poly(lactic-co-glycolic acid) (PLGA) NPs loaded with coumarin 6 (C6) as
187 her the biodegradable polymer poly(lactic-co-glycolic acid) (PLGA) or the biocompatible polymer polye
188 his hypothesis by assembling poly (lactic-co-glycolic acid) (PLGA) particles loaded with thrombin and
189 the hypothesis that inhalable poly(lactic-co-glycolic acid) (PLGA) particles of sildenafil prolong th
190 use of nitrofurantoin loaded poly(lactic-co-glycolic acid) (PLGA) particles to improve delivery to i
193 Drug-free and drug-loaded poly(lactic-co-glycolic acid) (PLGA) sutures were fabricated by electro
194 ribe microspheres composed of poly(lactic-co-glycolic acid) (PLGA) that can encapsulate IPV along wit
196 g and releasing properties of poly(lactic-co-glycolic acid) (PLGA) were approached with the applicati
197 ng" nanoparticles composed of poly(lactic-co-glycolic acid) (PLGA) with bright, spectrally defined qu
198 en as a model therapeutic and poly(lactic-co-glycolic acid) (PLGA) with similar molecular weight as t
199 priate biodegradable polymer (poly(lactic-co-glycolic acid) (PLGA)), utilization of a pH- and pore-mo
200 rofile for the degradation of poly(lactic-co-glycolic acid) (PLGA), a member of the most widely used
201 encapsulation of the drug in poly(lactic-co-glycolic acid) (PLGA), a polymer that is used in childre
202 lymeric implant made from poly(D,L-lactic co glycolic acid) (PLGA), and can be used as a guiding refe
203 ing biocompatible polymer poly(D,L-lactic-co-glycolic acid) (PLGA), ionizable lipid, helper lipid, an
206 meter of 227nm, composed of a poly(lactic-co-glycolic acid) (PLGA)-based core coated with poly(vinyl
208 mployed to manufacture porous poly(lactic-co-glycolic acid) (PLGA)-based intravitreal implants loaded
209 geting miRNA-155 and employed poly(lactic-co-glycolic acid) (PLGA)-based nanoparticle formulation for
210 study, we designed EDV-loaded poly(lactic-co-glycolic acid) (PLGA)-based polymeric nanoparticles (NP-
211 ed nanoparticles (NPs) of poly(D,L-lactic-co-glycolic acid) (PLGA)-poly(ethylene glycol) (PEG)-functi
213 with distinct functions: (i) poly(lactic-co-glycolic acid) (PLGA, P) serving as the main delivery pl
214 olyethylene glycol)-block-poly(D,L-lactic-co-glycolic acid) (PLGA-b-PEG-b-PLGA) sol-gels have been ex
215 ly(ethylene glycol)-block-poly(d,l-lactic-co-glycolic acid) (PLGA-b-PEG-b-PLGA) thermosensitive gel (
216 osed of end-to-end linkage of poly(lactic-co-glycolic-acid) (PLGA), polyethyleneglycol (PEG), and the
217 formulations as well as with poly(lactic-co-glycolic acid)(PLGA)-based microparticles, co-loaded wit
218 id)-b-poly(ethylene glycol)-b-poly(lactic-co-glycolic acid); PLGA-PEG-PLGA) for increasing the retent
219 nd low Mw free acid end-group poly(lactic-co-glycolic acids) (PLGAs) used to achieve continuous pepti
220 of poly(butylcyanoacrylate), poly(lactic-co-glycolic acid), poly(lactic acid) NPs, liposomes and ino
221 peripheral blood EPCs were seeded onto poly (glycolic acid)/poly (4-hydroxybutyrate) scaffolds for 5
222 ured on hydroxyapatite-coated poly(lactic-co-glycolic acid)/poly(L-lactic acid) (HA-PLGA/PLLA) scaffo
223 with a blend of FDA-approved poly lactic-co-glycolic acid-polyethylene glycol (PLGA_PEG) polymer mic
224 into a drug-encapsulating Poly dl-lactic-co-glycolic acid polymer (PLGA), via a double emulsion solv
225 a unique hexadentate-polyD,L-lactic acid-co-glycolic acid polymer chemically conjugated to PD98059,
226 S contrast agent composed of poly-lactide-co-glycolic acid polymeric (PLGA) microspheres (2-micron di
227 stinct compartments namely; poly(l-lactic-co-glycolic acid) polymeric core acting as a drug reservoir
230 an random copolymers with the same lactic to glycolic acid ratios as demonstrated by molecular weight
231 ain an ester linkage between a threonine and glycolic acid residue and an N-terminal FITC fluorophore
233 Self-healing of pores in Poly(lactic-co-glycolic acid)s (PLGA) plays an important role in the en
234 at hydrolytic degradation of poly(lactic- co-glycolic acid)s is dramatically affected by sequence.
235 lylysine around a salt-leached polylactic-co-glycolic acid scaffold that is degraded in a sodium hydr
236 orated in a uniquely designed poly(lactic-co-glycolic) acid scaffold, a clinically safe polymer, foll
237 al (3D)-printed biodegradable poly(lactic-co-glycolic acid) scaffolds (PLGA), and hydroxyapatite powd
238 Specifically labeled deuterated lactic and glycolic acid segmers were likewise prepared and polymer
239 bic acid (AA) in the core and poly(lactic-co-glycolic acid) shell incorporating iron oxide nanocubes
241 he OS studied include the potassium salts of glycolic acid sulfate, hydroxyacetone sulfate, 4-hydroxy
244 ion as a synthetic equivalent to the dipolar glycolic acid synthon, the glyoxylate anion synthon, or
245 ibes the use of silyl glyoxylates as dipolar glycolic acid synthons in a controlled oligomerization r
246 icle formulations composed of poly lactic-co-glycolic acid take too long to release encapsulated payl
247 amidoamine dendrimers and poly(d,l-lactic-co-glycolic acid) that demonstrate adjuvant properties in v
249 the synthesis of alternating poly(lactic-co-glycolic acid) via a regioselective ring-opening polymer
251 of 90% hydroxyapatite and 10% poly(lactic-co-glycolic acid) were printed using a microextrusion proce
252 n-approved 500nm carboxylated-poly(lactic-co-glycolic) acid, were infused intravenously into wild-typ
253 e developed a scaffold from variants of poly(glycolic) acid which were braided and coated with an ela
254 ne cores and shells made from poly(lactic-co-glycolic acid) with varying degradability kinetics-for t
255 Nanoparticles composed of poly(lactic-co-glycolic acid), with polyethylene glycol coatings to res