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1 tion that converts the polyCBL into a linear polyester.
2 e incorporation of C(16) monomers into cutin polyester.
3 t and the existence of an extended aliphatic polyester.
4 to give the corresponding highly alternating polyester.
5 uorescein during enzymatic hydrolysis of the polyester.
6 tween the structures and properties of these polyesters.
7 approach to generate well-defined functional polyesters.
8 lymerized into the corresponding unsaturated polyesters.
9 containing no protic groups into unsaturated polyesters.
10 lity to hydrolyse both natural and synthetic polyesters.
11 ion efficiency of semi-crystalline bio-based polyesters.
12 ed to convert dimethacrylates to unsaturated polyesters.
13 ng well-defined high molecular weight cyclic polyesters.
14 sis of increasingly complex and well-defined polyesters.
15  in several monomers of cell wall-associated polyesters.
16  for hydrolysis of small molecule esters and polyesters.
17 s a strategy to generate well-defined cyclic polyesters.
18  monomers derived from non-extractable lipid polyesters.
19 merous types of functionality onto aliphatic polyesters.
20 ethane generated the homologated nitroalkane-polyesters.
21 ted to produce hydrogen gas or biodegradable polyesters.
22 stalline ester-linked COFs related to common polyesters.
23 g the trehalose- and zwitterion- substituted polyesters.
24 ated to hydrolyze all structurally different polyesters.
25 o prepare clinically translatable degradable polyesters.1 A variety of functional groups have been in
26 d with disperse blue 3 and disperse blue 14, polyester 777 dyed with disperse red 1 and disperse red
27 lypropylene (25%), polyacrylamides (10%) and polyester (8.3%).
28 es were overexpressed together the epidermal polyesters accumulated new C20 and C22 omega-hydroxyacid
29  finishes, acrylic melamine (clear coating), polyester acrylic melamine (white coating) automotive fi
30 pecifically, two isomeric arylene-ethynylene polyesters afforded significantly different product dist
31 ed (DB, 50%), and pseudodendritic (DB, 100%) polyesters allowing the establishment of architecture ca
32 achieved using a hybrid polydimethylsiloxane/polyester amperometric lab-on-a-chip (LOC) microsystem w
33 an oxidant mechanism, whereas the non-coated polyester analogue and the Pluronic F68 alone had no eff
34  ingestion of a range of polymers, including polyester and acrylic fibers.
35 e systematically investigated the effects of polyester and carboxylesterase structure on the hydrolys
36  this work highlights the importance of both polyester and carboxylesterase structure to enzymatic po
37 le fibres with high tensile strength such as polyester and nylon.
38 tic slings, particularly those made of woven polyester and other tightly woven material erode 15 time
39 ow reactors to rapidly generate libraries of polyester and polycarbonate homopolymers and block copol
40 imple but robust strategy to bond semiporous polyester and polycarbonate membranes between layers of
41 lcohol)(PVA) sizes for high-speed weaving of polyester and polyester/cotton yarns to substantially de
42 es were significantly greater in cotton than polyester and similar for BFRs and high molecular weight
43 conjugation of hydroxyl-containing agents to polyesters and formation of corresponding nanoparticles.
44                                              Polyesters and polyamides are very suitable to be depoly
45 lutarate, an attractive C5 building block of polyesters and polyamides.
46 is of relevant general purpose and specialty polyesters and polyamides; some of them are currently de
47 ynthetic routes to convert these monomers to polyesters and polycarbonate, and the different end-of-u
48                                    Aliphatic polyesters and polycarbonates are a class of biorenewabl
49        Among potential candidates, aliphatic polyesters and polycarbonates are promising materials du
50  of metal-free polymers, including aliphatic polyesters and polyethers, poly(alpha-peptoid)s, poly(me
51 me-mediated hydrolysis of aliphatic-aromatic polyesters and will therefore have important implication
52 d 75% for rayon, 71.2% for cotton, 81.3% for polyester, and 53.2% for calcium alginate.
53                                              Polyester apparel accounts for a large proportion of the
54                                Biodegradable polyesters are being increasingly used to replace conven
55                                              Polyesters are extensively used in drug delivery because
56                                The resulting polyesters are highly alternating and have high molecula
57              The roles of cutin- and suberin polyesters are often attributed to their dominant alipha
58 mbly of a new class of amphiphilic aliphatic polyesters are presented.
59 ew class of bio-based fully degradable block polyesters are pressure-sensitive adhesives.
60                         Degradable aliphatic polyesters are the cornerstones of nanoparticle (NP)-bas
61                                Water-soluble polyesters are used in a range of applications today and
62  nanoparticle core functionalized with eight polyester arms.
63 pplication and success of hydroxy acid based polyesters as degradable sutures and controlled drug del
64 reaction are shown to be compatible with the polyester backbone, this method is a generally useful me
65 y(aminoesters) with N-acylated amines in the polyester backbone.
66                                  A series of polyesters based on 2-propargyl-1,3-propanediol or 2,2-d
67       A similar series of aromatic-aliphatic polyesters based on diethyl-2,5-furandicarboxylate and o
68             In this regard, the synthesis of polyesters based on the natural polyhydroxyalkanoate (PH
69 sulated into biocompatible and biodegradable polyester-based nanoparticles.
70                     Although many studies on polyester biodegradability have focused on aerobic envir
71 zymes and aquatic microorganisms involved in polyester biodegradation and mineralization.
72 hich is considered the rate-limiting step in polyester biodegradation.
73 ases is considered the rate-limiting step in polyester biodegradation.
74 ide evidence for a critical role of GPAT5 in polyester biogenesis in seed coats and roots and for the
75  knockout mutant lines for genes involved in polyester biosynthesis (att1, fatB and gpat5) were exami
76 substrate specificities (1) strongly support polyester biosynthetic pathways in which acyl transfer t
77 lonyl-CoA reductase applied for biotechnical polyester building block synthesis.
78 d or distinguished unreacted monomers in the polyester bulk in contrast to acid-base titrations where
79 tive analysis of the hydrolysis of two model polyesters by eight different carboxylesterases revealed
80  the enzymatic hydrolysis of eight aliphatic polyesters by two fungal esterases (FsC and Rhizopus ory
81 roval of the fat substitute olestra (sucrose polyester) called for active postmarketing surveillance
82 er, monomer diversity in naturally occurring polyesters can be limited with respect to the design of
83        The results obtained suggest that new polyesters can be synthesized with desirable properties
84 yl azide, namely CF3(CF2)7CH2CH2N3, to yield polyesters carrying long-chain alkylene segments in the
85      In the current study, beta-cyclodextrin polyester (CDPE) hydrogels serve as sacrificial macropor
86 stribution of the acid components within the polyester chain ((1)H NMR).
87 ed to a combination of temperature-dependent polyester chain flexibility and accessibility of the enz
88  the catalytic site of RoL due to increasing polyester chain mobility.
89    Hydrolyzability increased with increasing polyester-chain flexibility as evidenced from difference
90         With PEDOT:PSS coated onto cellulose/polyester cloth, the SC shows specific capacitance of 8.
91 mutants in which the abundance of cutin, the polyester component of the cuticle, was strongly reduced
92                         Acylsugars are sugar-polyesters composed of saturated, un-saturated, and vari
93                               These AB block polyesters comprise polycaprolactone (hydrophobe) and an
94      The stigmatic estolide is a lipid-based polyester constituting the major component of exudate in
95 annel layer between uncoated cover sheets of polyester containing precut access holes.
96                                 For example, polyesters containing 1,2-ethanediol were hydrolyzed fas
97 g 1,2-ethanediol were hydrolyzed faster than polyesters containing 1,8-octanediol.
98 It was found that increasing the hydrophobic polyester content in the hydrogel reduced the swelling v
99 nce the use of synthetic fabrics, especially polyester, continues to increase.
100  carbonate-co-caprolactone), and a cellulose/polyester core.
101                             Here, cotton and polyester-cotton fabrics were sonochemically coated with
102              Two fabrics [polyamide (PA) and polyester/cotton (PES/CO)] were selected and coated with
103  PVA and chemically modified starch sizes on polyester/cotton fabrics, and had relative weaving effic
104 izes for high-speed weaving of polyester and polyester/cotton yarns to substantially decrease environ
105 astic, and porous crosslinked urethane-doped polyester (CUPE) scaffold sheets that are bonded togethe
106  protective cuticle, largely composed of the polyester cutin.
107  hexadecanoic acid, a monomer of the cuticle polyester, cutin.
108                              A biocompatible polyester dendrimer composed of the natural metabolites,
109                  An asymmetric biodegradable polyester dendrimer containing 8-10 wt % DOX was prepare
110                                              Polyester dendrimers are attractive for in vivo delivery
111 ly suitable for the synthesis of custom-made polyester dendrimers.
112 e research activities generated on aliphatic polyester dendritic architectures based on bis-MPA.
113 d lipase activity, and seven proteins showed polyester depolymerization activity against polylactic a
114                                              Polyester deposition was followed over Brassica seed dev
115 led the rapid synthesis of >130 lipocationic polyesters directly from functional monomers without pro
116      The other functionalities in the linear polyester do not participate in the nanoparticle formati
117 t cationic proto-peptides (depsipeptides and polyesters), either produced as mixtures from plausibly
118 the aliphatic load in both suberin and cutin polyesters essentially remained unaffected.
119                  Polybutylate-coated braided polyester (Ethibond* 5-0) suture is a safe and effective
120 tenolol deposited on glass, wood, steel, and polyester fabric.
121                      Over 30 days cotton and polyester fabrics accumulated 3475 and 1950 ng/dm(2) sum
122 d by dip-coating acrylic, cotton, nylon, and polyester fabrics from solutions of diluted rat blood.
123 elative weaving efficiency similar to PVA on polyester fabrics, although with 3- 6% lower add-on.
124 nsulation panel made by hemp fiber (85%) and polyester fiber (15%) in 1 m(2) of wall having a thermal
125 ere, in combination with the stainless steel/polyester fiber blended yarn, the polydimethylsiloxane-c
126 cs may explain the observed results in which polyester fibers and polyamide beads triggered the most
127 h) and chronic (8 d) effects of microplastic polyester fibers and polyethylene (PE) beads on freshwat
128 ber composites reported to date, the MOF-808/polyester fibers exhibit the highest rates of nerve agen
129 ial distribution of local stresses in single polyester fibers under uniaxial strain.
130  the effects of six different microplastics (polyester fibers, polyamide beads, and four fragment typ
131 ere aligned with an intermediary cut-through polyester film and then thermally laminated together at
132 phic software package and laser printed on a polyester film.
133  by integrating cellulose paper and flexible polyester films as diagnostic biosensing materials with
134 olymer, and the laser-printing of toner onto polyester films has been shown to be effective for gener
135 tructure on the hydrolysis of nanometer-thin polyester films using a quartz-crystal microbalance with
136 een 20 and 1000 times more formaldehyde than polyester filters under similar RH and airflow condition
137   Formaldehyde emissions from fiberglass and polyester filters used in building heating, ventilation,
138 olyester insulation) and one off-brand (100% polyester fleece).
139 -brand clothing manufacturer (three majority polyester fleece, and one nylon shell with nonwoven poly
140 sing a greater diversity of VOCs compared to polyester foam.
141 rs in the commercialization of the bio-based polyesters, for example polyhydroxyalkanoates synthesize
142 rably with commercial adhesives or bio-based polyester formulations but without the need for tackifie
143 caprolactone (hydrophobe) and an alternating polyester from succinic acid and an ether-substituted ep
144 s in which a CO2 laser is used to remove the polyester from the channel sections of the internal laye
145 ologically important biodegradable aliphatic polyesters from cyclic esters or lactones.
146                                              Polyester garments with different textile characteristic
147 he usage of ionic liquids for studying plant polyesters has advantages over conventional approaches,
148                    The resulting unsaturated polyesters have a high thermal stability and can be read
149                                Biodegradable polyesters have a large potential to replace persistent
150                                Biodegradable polyesters have the potential to replace nondegradable,
151 reening and mechanistic studies of enzymatic polyester hydrolysis.
152  and carboxylesterase structure to enzymatic polyester hydrolysis.
153 . were chosen for in-silico screening toward polyester hydrolyzing enzymes.
154 ysis included increased water solubility and polyester hydrophilicity as well as shorter diol chain l
155 in the extracellular deposition of the cutin polyester in the tomato fruit cuticle.
156 here is much less known on biodegradation of polyesters in natural and artificial anaerobic habitats.
157 iacylglycerol-/diacylglycerol-based estolide polyesters in the petunia stigma.
158                            Although used for polyesters in this investigation, SEED-ROMP represents a
159 understanding of biodegradation processes of polyesters in WWTPs where the extracellular enzymatic hy
160 er fleece, and one nylon shell with nonwoven polyester insulation) and one off-brand (100% polyester
161                        A series of sulfonate polyester ionomers with well-defined poly(ethylene oxide
162                            Data generated by Polyester is a reasonable approximation to real RNA-seq
163                                              Polyester is an R package designed to simulate RNA-seq d
164  high-molecular-weight metal-free recyclable polyester is reported.
165                  Preparation of an unzipping polyester is reported.
166 d with the outer integument and a cutin-like polyester layer associated with the inner seed coat.
167 noparticles that have a gold core, an apolar polyester layer for drug loading, a polar PEO corona to
168 parel accounts for a large proportion of the polyester market, and synthetic jackets represent the br
169 y step during the breakdown of biodegradable polyester materials in natural and engineered systems.
170 functionalized well-defined 3-D nanoparticle polyester materials in targeted nanoscopic ranges with a
171 lcanivorax to clear marine environments from polyester materials of anthropogenic origin as well as o
172 rious functionalities or by mixing different polyester materials to achieve controlled amounts of spe
173 ty and can be readily cross-linked to robust polyester materials.
174 le, a protective layer composed of the cutin polyester matrix and cuticular waxes.
175 DL), a fluorogenic ester substrate, into the polyester matrix and on monitoring the enzymatic cohydro
176 for hydrolysis of the protective cutin lipid polyester matrix in plants and thus have been exploited
177 y epidermal cells and is composed of a cutin polyester matrix that is embedded and covered with cutic
178                        Samples of biomedical polyester (Max-Prene 955) and a fluoropolymer (polyvinyl
179 ased with decreasing differences between the polyester melting temperatures and the experimental temp
180 al hernia were randomized to a self-gripping polyester mesh or a sutured polyester mesh.
181  a self-gripping polyester mesh or a sutured polyester mesh.
182 hanically fragmented and size filtered using polyester meshes.
183 nonrecyclable waste-including microplastics (polyester microfibers) and food-contaminated plastic-and
184 ted microfluidic system using a multilayered polyester microfluidic disc created through laser print,
185 n the portal trunk of C57BL6 adult mice with polyester microspheres, to ensure a bilateral and distal
186 aphy coupled with mass spectrometry of lipid polyester monomers confirmed a drastic decrease in aliph
187                              The variance in polyester monomers of these mutants is correlated with d
188 ent the synthesis of discrete functionalized polyester nanoparticles in selected nanoscale size dimen
189 We report the synthesis and encapsulation of polyester nanosponge particles (NPs) co-loaded with tamo
190 nsely cross-linked and hydrolytically stable polyester networks with low soluble fractions can be obt
191 eting ligands are required, these functional polyester NPs provide an exciting alternative approach f
192  cells internalized both coated and uncoated polyester NPs to a similar extent, with uptake observed
193 hemicals used in the production of plastics, polyesters, nylons, fragrances, and medications.
194  structure and formation of this hydrophobic polyester of glycerol and hydroxy/epoxy fatty acids has
195       The plant cuticle consists of cutin, a polyester of glycerol, hydroxyl, and epoxy fatty acids,
196 of apparently all plant cuticles is cutin, a polyester of hydroxy fatty acids; however, despite its u
197              The most intriguing unsaturated polyester of the series is that based on the biomass-der
198                               Acylsugars are polyesters of short- to medium-length acyl chains on suc
199                             In this study, 5 polyesters of similar molar mass were synthesized by rea
200 vidual dye-modified copolymers, dye-modified polyesters offer advantages over physical entrapment of
201                It occurs as an extracellular polyester on the aerial surface of all plants, provides
202           The most abundant polymer type was polyester or polyethylene terephthalate at 71%, followed
203                                  With Dacron polyester or rayon-tipped swabs, there was no consistent
204  enables the selective preparation of either polyesters or polycarbonates or copoly(ester-carbonates)
205                     Calcium alginate, Dacron polyester, or rayon-tipped swabs were inoculated with pn
206 L, thereby producing exclusively unsaturated polyester P(MBL)ROP with Mn up to 21.0 kg/mol.
207 -poly(ethylene glycol) (PEG) based precision-polyester (P2s) platform, permitting 5-12 periodically s
208 ludge to hydrolyze the synthetic compostable polyester PBAT (poly(butylene adipate-co-butylene tereph
209 merization (ROP), generated their respective polyesters (PE) or poly(ester amides) (PEA).
210  (PE) and polystyrene (PS) microspheres, and polyester (PEST) fibers).
211 crylate) (PMMA), polyethylene terephthalate (polyester, PET), and PETG are explored as substrate opti
212 hate (polyP), and the amphiphilic, solvating polyester, poly-(R)-3-hydroxybutyrate, frequently associ
213 ach may be expanded to a wide range of other polyester, polyamide, and polyurethane platform material
214 al behavior, and degradability of long-chain polyester, polyamides, polyurethanes, polyureas, polyace
215 il biodegradable mulch films composed of the polyester polybutylene adipate-co-terephthalate (PBAT) a
216 vity toward the degradation of the synthetic polyester polycaprolactone.
217   Vaginal fluid specimens were collected via polyester/polyethylene terephthalate swabs every other m
218                                   Suberin, a polyester polymer in the cell wall of terrestrial plants
219 lymers, such as polysaccharides, polyamides, polyesters, polyphosphates, extracellular DNA and protei
220 degradable synthetic polymers (polypeptides, polyesters, polyphosphazenes, etc.).
221 copy identified multiple polymers, including polyester, polypropylene, polyvinyl chloride and vinyl c
222 orb crude oil microdroplets from water using polyester polyurethane (PESPU) foam.
223 f oligomers indicates the presence of linear polyesters possibly formed via esterfication reactions o
224                                          The polyester powder contained 6 pg/g and 2 pg/g for (232)Th
225 for SGs and acyl SGs in trafficking of lipid polyester precursors.
226 e the synthesis of closely related sequenced polyesters prepared by entropy-driven ring-opening metat
227                        The amphiphilic graft polyesters prepared in this study are shown to be biocom
228  well-defined and functionalizable aliphatic polyesters remains a key challenge in the advancement of
229 in wax and polycaprolactone, a biodegradable polyester reported for the first time floating in off-sh
230                                              Polyester represents one such polymer, and the laser-pri
231 ples to assess the degree of interference of polyester resin in the GC-MS and Carbon-IRMS signals of
232 molecular and isotopic biomarker analysis on polyester resin-impregnated sediment slabs from archaeol
233 ed epimerization of the alpha-carbon atom in polyesters resulting in the loss of isotacticity.
234  a CO(2) laser to create the microchannel in polyester sheets containing a uniform layer of printed t
235 nstructed by backfilling small holes made in polyester sheets using a CO2 laser etching system.
236 abundant and widespread monomer of the cutin polyester, show that the morphology of floral surfaces d
237 e overaccumulation of ferulate in lipophilic polyester significantly increased the tolerance of trans
238 on indium tin oxide-coated substrates (e.g., polyester) simply by solution-casting the ECL gel and br
239 nces that we attribute to differences in the polyester structure.
240 ng boards made of typical anhydride epoxy or polyester substrate.
241 ax in its natural environment, where natural polyesters such as polyhydroxyalkanoates (PHA) are produ
242                                 Conventional polyesters such as polylactide (PLA) or its copolymer, p
243                                              Polyester suture was more effective at lower K21 concent
244 cal lengths of surgical suture (chromic gut, polyester suture, silk, and nylon suture) and control un
245  The number of colonies from both the Dacron polyester swabs and medium were significantly lower than
246 culture, rayon swabs are superior and Dacron polyester swabs are inferior.
247 of cutin synthase-like (CUS) proteins act as polyester synthases with negligible hydrolytic activity.
248  as partners of fatty acyl oxidases in lipid polyester synthesis and indicate that their cooverexpres
249 ught molecular bases of alkane formation and polyester synthesis have allowed construction of nearly
250           Traditional chemical catalysts for polyester synthesis have enabled the generation of impor
251                       Recent developments in polyester synthesis have established several systems bas
252 esults reveal a conserved mechanism of cutin polyester synthesis in land plants, and suggest that ela
253 mmobilized enzyme-catalysts for condensation polyester synthesis.
254                                              Polyesters synthesized through the alternating copolymer
255                       Diverse functionalized polyesters, synthesized with pendant functionalities via
256  of the key requirements in semi-crystalline polyesters, synthetic or bio-based, is the control on cr
257 rward technique that can be applied to other polyester systems without major alterations.
258 for the semiquantitative characterization of polyester systems.
259 eads, and four fragment types: polyethylene, polyester terephthalate, polypropylene, and polystyrene)
260 ters on the release of microfibers (MF) from polyester textiles was studied.
261 microplastic fibers released from synthetic (polyester) textiles during simulated home washing under
262 normous potential for biodegrading aliphatic polyesters thanks to a unique and abundantly secreted al
263  WIN1 influences the composition of cutin, a polyester that forms the backbone of the cuticle.
264 lenge, we report the discovery of functional polyesters that are capable of delivering siRNA drugs se
265 lic anhydride comonomer results in amorphous polyesters that exhibit glass transition temperatures (T
266 cturally different ionic phthalic acid based polyesters (the number-average molecular weights (Mn) 17
267 al approach to study enzymatic hydrolysis of polyesters, the key step in their overall biodegradation
268 lthough aromatics are the minor component of polyesters, they play important role in the sealing func
269 n of changes in the masses and rigidities of polyester thin films during enzymatic hydrolysis using a
270             Chemical release from cotton and polyester to laundry water was >80% of aliphatic OPEs (l
271 rovide biosynthetic access to alpha-branched polyesters to enrich the properties of bio-based sustain
272 as been shown to be effective for generating polyester-toner (PeT) microfluidic devices with channel
273     Here, we describe the use of inexpensive polyester-toner, rotation-driven microfluidic devices wi
274             We describe the integration of a polyester track-etched (PETE) nanofluidic interface to p
275 lyethylene glycol (PEG-PBA-PEG) (1.0-4.0 mg) polyester triblock copolymer; food oil, using olive and
276 study was to apply an elastic, biodegradable polyester urethane urea (PEUU) cardiac patch onto subacu
277           The vast majority of tapes contain polyester-urethane as the magnetic particle binder, the
278 nomers, which were used to prepare iodinated polyesters using a pre-functionalization approach.
279 he hydrolysis rates and extents of aliphatic polyesters varying in the length of their dicarboxylic a
280 ly(butylene adipate-co-terephthalate) (PBAT) polyesters varying in their terephthalate-to-adipate rat
281 pylene oxide, we synthesized semicrystalline polyesters via the copolymerization of a range of epoxid
282                     The best DL for blood on polyester was found in the mid-IR spectral window corres
283             In this work, a blend of PLA and polyester was studied and its volatile composition in th
284                        Activities on all the polyesters were also confirmed with the strains P. pseud
285 h high performing zwitterionic and trehalose polyesters were also degraded, and the polymers and degr
286 ing the corresponding diacid chloride; these polyesters were quantitatively "clicked" with a fluoroal
287 ee types of swabs, flocked-nylon, rayon, and polyester, were evaluated by 3 extraction methods, the s
288 e highest HTP activity and also produced the polyester with the highest Mn, while the Cl-substituted
289 ontrolled coupling of epoxide functionalized polyesters with 2,2'-(ethylenedioxy)bis(ethylamine) to g
290 rs are efficiently polymerized to make block polyesters with controlled compositions.
291 afford structurally and functionally diverse polyesters with controlled molecular weights and dispers
292 -based system rapidly converts gamma-BL into polyesters with high monomer conversions (up to 90 %), h
293 is a route to a new class of semicrystalline polyesters with improved properties, produced from readi
294 t with secondary alcohol groups and produces polyesters with lower molecular size.
295 ide leads to a new class of high-performance polyesters with tunable mechanical properties.
296 ected and assigned to free acids, esters and polyesters with up to eight units.
297 erize the architecture of aromatic-aliphatic polyesters with varying degrees of branching.
298 rovides access to a range of new unsaturated polyesters with versatile functionality, as well as the
299                        The location of these polyesters within the seed coat, and their contributions
300 e alkyne groups at high density in aliphatic polyesters without compromising their crystallinity via

 
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