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1 apsulated within the hydrophilic core of the liposome.
2 ance association of chaperone-free CHIP with liposomes.
3  doxorubicin across the lipid bilayer of the liposomes.
4 e kinetics of doxorubicin leakage from Doxil liposomes.
5 f small interfering RNA (siRNA) and cationic liposomes.
6 ly disordered proteins (IDPs), peptides, and liposomes.
7 earch of candidate APIs for delivery by nano-liposomes.
8 osomes can be enhanced using ligand-targeted liposomes.
9 vent along with lateral interactions between liposomes.
10  transport assays on ZntB reconstituted into liposomes.
11 of noncovalent linkage of the trimers to the liposomes.
12 driven proton pump proteorhodopsin (PR) into liposomes.
13 ly used for modelling the oxidation curve of liposomes.
14 concentric, pericentric and multicompartment liposomes.
15 bution, zeta potential and morphology of the liposomes.
16  of 1,2-dioleoyl-sn-glycero-3-phosphocholine liposomes.
17 from yeast and incorporated the complex into liposomes.
18 ave used here assays of calcein release from liposomes.
19 stribution and decrease in clearance for the liposomes.
20 ctron cryotomography in several bacteria and liposomes.
21 COPII complex, which binds "major-minor-mix" liposomes.
22 g was much lower than that achieved with the liposomes.
23 membrane (TM) helices in a CitA construct in liposomes.
24 lpha-helical conformation in the presence of liposomes.
25 rect delivery of ATP into HCT116 cells using liposomes.
26 ed liposomes to +45.5mV in biopolymer-coated liposomes.
27  cleavage and released Ca(2+) from preloaded liposomes.
28 7 binds to PS but not to phosphatidylcholine liposomes.
29 lymers in generating stable, surface neutral liposomes.
30 as well as permeabilization of PA-containing liposomes.
31  and size to be similar to those of Doxil(R) liposomes.
32 on of de novo designed (AALALAA)3 helices in liposomes.
33  rapid transbilayer phospholipid exchange in liposomes.
34 mproved in vitro stability over nickel-based liposomes.
35 n, immobilized on membranes, or presented in liposomes.
36 mmonium propane (DOTAP) and the zwitterionic liposome 1,2-Dioleoyl-sn-Glycero-3-Phosphoethanolamine (
37 omplexes were prepared and encapsulated into liposomes (ACL).
38                       Compared to ANE-loaded liposomes, ACL-90H, ACL2-90H and ACL2-S100 displayed sig
39                            ANE-double-loaded liposomes (ACL2) were obtained with the HP-beta-CD/ANE c
40  how the affinity and valency of dual-ligand liposomes affect the binding and selectivity of delivery
41              Our data show that protein-free liposomes, after variable delay times, are captured by t
42 ts in (i) bulk soybean oil, (ii) soybean oil liposomes and (iii) soybean-oil/water emulsions.
43                        Our results show that liposomes and chromaffin granules fuse with GUVs contain
44  is also sensitive to the motion of adsorbed liposomes and coupled solvent along with lateral interac
45 etween ion transport abilities in artificial liposomes and cytotoxic activity on human cancer cell li
46 d mammalian GIRK2 channels incorporated into liposomes and demonstrate that cholesterol or intoxicati
47 , biological soft-matter particulates (e.g., liposomes and exosomes) adsorbed at a solid-liquid inter
48 xidant properties of the bioactive extracts, liposomes and in vitro digested surimi gels were determi
49 ic-co-glycolic acid), poly(lactic acid) NPs, liposomes and inorganic systems.
50 eptides, spherical nucleic acids, deformable liposomes and liquid crystalline nanodispersions.
51 (2+), while Mg(2+) has no effect with 100 nm liposomes and modest effect with giant unilamellar vesic
52  planar membranes, and thus, it is absent in liposomes and not detectable in calorimetric measurement
53  of bound ligands, we additionally label the liposomes and perform dual-color fluorescence cross-corr
54 n as stable, monodisperse, and biocompatible liposomes and polymersomes called for the elaboration of
55  lipid- and polymer-encapsulated containers, liposomes and polymersomes, respectively.
56 lamellar crystals and their structure mimics liposomes and polymersomes.
57 ed field of nanoparticle membrane-loading of liposomes and polymersomes.
58 -coil formation, the C-terminal domain bound liposomes and ProP concentrated at the cell poles in a C
59  substantially decreased the accumulation of liposomes and silicon particles in the mononuclear phago
60 ntribute to the enhanced accumulation of the liposomes and small molecule probe.
61 for incorporation into lipophilic regions of liposomes and subsequent in vitro delivery to cells, are
62 re also released from the aqueous chamber of liposomes and taken up into tumor cells to enhance the p
63 d by the in vitro transcription in "nucleus" liposomes and the mimicry of the architecture of eukaryo
64 on with LE against oxidation of peroxidating liposomes and with QC showing the largest effect.
65 an be used both in detergent micelles and in liposomes, and contain red-shifted fluorophores that are
66 riments were performed for Doxil, Doxil-like liposomes, and Doxil-like liposomes with reduced cholest
67  versions, and other single amphiphiles into liposomes, and from block copolymers into polymersomes.
68 cles, liquid-filled, bilayer-coated vesicles/liposomes, and gas-filled bubbles.
69 he membrane bending energy for the gel-phase liposomes, and the results are consistent with literatur
70 consisting of synthetic or natural polymers, liposomes, and virus-like particles as well as nonbiodeg
71                                              Liposomes are an attractive option due to their low toxi
72 iments with purified AQP0 reconstituted into liposomes are challenging because the water permeability
73                                        Doxil liposomes are designed to retain doxorubicin in circulat
74                                              Liposomes are lipid based bilayer vesicles that can enca
75                                              Liposomes are nanoparticles used in drug delivery that d
76                                     Finally, liposomes are ruptured by methanol and the released-dopa
77 egatively charged lipid-based nanoparticles (liposomes) are derived from combined analysis of exchang
78 r structures (oligonucleotides, peptides and liposomes) are formed under the same phosphorylation rea
79 Artificial membrane-bound vesicles, known as liposomes, are versatile tools for modelling biological
80 tier 2) 16055 virus following inoculation of liposome-arrayed trimers.
81 s via permeation across lipid nanoparticles (liposomes) as a mimicry of biological membranes.
82 he surface, core, and bilayer regions of the liposomes, as determined by electrical charge (zeta-pote
83 onstitution of membrane-protein binding in a liposome assay shows that the mechanism involves protein
84                         Although in vitro MA-liposome association is influenced by disparate variable
85                                              Liposome association of peptides representing the C-term
86                  When incubated with anionic liposomes at pH 5, full-length and the C-terminal part o
87 ent analysis revealed two separate phases of liposome autoxidation.
88                                    Cell- and liposome-based assays demonstrated that GSDMD pores were
89                                        Using liposome-based assays, we show that Ca(2+) binding to C2
90 ) mice, delivery of stabilized siRNA using a liposome-based carrier targeted approximately 95% of HSC
91 olved, despite the importance in translating liposome-based drug delivery systems to other molecules
92  present achievements in: (i) preparation of liposome-based formulations of various PAs, (ii) develop
93               Therapeutic potential of these liposome-based PAs has been demonstrated successfully in
94                                          All liposome batches were nanometric oligolamellar-type vesi
95 antibody titers than the soluble trimers and liposome-bearing trimers via noncovalent linkages.
96                                              Liposome binding trends observed using a recently develo
97  a quantitative understanding of dual-ligand liposome binding, the insights gained from this study ca
98 of 97-100% and 98-100% respectively, and the liposome biodistribution was imaged by PET for up to 8da
99                                PS-containing liposomes blocked HCV cell attachment and subsequent HCV
100               Cross-linking experiments with liposome bound Atg18 yielded several PE cross-linked pep
101 ence of detergent and does not take place in liposomes but in mixed micelles.
102 g and covalent linkage of the trimers to the liposomes by reengineering the polyhistidine tail to inc
103 ieve the desired high concentrations in nano-liposomes by remote loading.
104                               Moreover, such liposomes can be directed to mitochondria expressing sim
105 the alphavbeta6 receptor, cellular uptake of liposomes can be enhanced using ligand-targeted liposome
106 ition, fusion or subsequent acidification of liposomes can be monitored by incorporation of appropria
107 rbents, and A2AR assimilation into synthetic liposomes can be visualized by microscopy and probed by
108 oxorubicin delivery by temperature-sensitive liposomes can reliably cure local cancer in mouse models
109    Here we show that lipid bilayer vesicles (liposomes) can be triggered to release an encapsulated m
110            Our first-generation nickel-based liposomes captured HIV-1 Env glycoprotein trimers via a
111                 In particular, the maleimide liposomes captured HIV-1 Env trimers via a more stable c
112                    Purified EMC in synthetic liposomes catalyzed the insertion of its substrates in a
113        The incorporation of the freeze-dried liposomes caused a slight decrease in gel strength and c
114 ventional liposomes (CL) and HP-ss-CD-loaded liposomes (CDL).
115 philic AMD3100 was released from the aqueous liposome chamber and then bound with CXCR4 receptors on
116 chitecture), and drug loading in determining liposome characteristics.
117 somal formulations were tested: conventional liposomes (CL) and HP-ss-CD-loaded liposomes (CDL).
118 osomes that persisted several days after the liposomes cleared from blood.
119 cted that injection of clodronate-containing liposomes (CLs), which selectively deplete cells efficie
120  the domain in the presence of ubiquitin and liposomes combined that are not observed with either lip
121 ed complex was then stabilized with cationic liposomes composed of DOTAP (2, 3-Dioleoyloxy-propyl)-tr
122                                              Liposomes composed of lipids containing head groups of p
123       To achieve this objective, a series of liposome compositions that contained various concentrati
124                                          The liposomes consist of single bilayers, as demonstrated by
125 transmembrane asymmetry of small unilamellar liposomes consisting of zwitterionic and charged lipids
126                    The results indicate that liposomes constitute a suitable system for encapsulation
127 -dioleoyl-sn-glycero-3-phosphocholine (DOPC) liposomes contacting a titanium dioxide substrate.
128                        Fine-disperse anionic liposomes containing black mulberry (Morus nigra) extrac
129 ed fusion of VAMP8-containing liposomes with liposomes containing exocytic or endosomal Q-SNAREs and
130 diffusing particles, including nanodiscs and liposomes containing membrane protein receptors.
131  conjugated to tetanus toxoid and mixed with liposomes containing monophosphoryl lipid A as an adjuva
132 t rVapA(32-189) interacted specifically with liposomes containing phosphatidic acid in vitro.
133 eloped a long-circulating Dox formulation in liposomes containing small amounts of porphyrin-phosphol
134                                When assaying liposomes containing sphingomyelin and cholesterol, we o
135  addition, the GSDMB N-terminal domain binds liposomes containing sulfatide.
136 mplex, as compared to incubation with intact liposomes containing the complex.
137  that incorporation of alpha-tocopherol into liposomes contributes a significant antioxidant effect o
138          Notably, in comparison to synthetic liposomes covalently coupled with hEGF, it is demonstrat
139             Dual-targeting heteromultivalent liposomes covered with polyethylene glycol (PEG) were sy
140 es in the extent of ionic strength-modulated liposome deformation at both low and high surface covera
141 lent samples were qualitatively sensitive to liposome deformation only at saturation coverage.
142 ent discrimination arises from the extent of liposome deformation, while the QCM-D measurements yield
143                                              Liposome-delivered 5(6)-carboxy-DCFH2 enabled real-time
144 cy in A549 xenograft model in mice, both the liposomes demonstrated excellent tumor suppression and r
145                            Biopolymer-coated liposomes demonstrated more sustained peptide release be
146  principle study using F/R incorporated into liposomes, designed to target inflamed endothelium, show
147 s in Lactococcus lactis and in reconstituted liposomes directly demonstrated that SLC25A3 functions a
148 A delivery to the airways that consists of a liposome (DOTMA/DOPE; L), an epithelial targeting peptid
149 d a prediction of drug leakage from the nano-liposomes during storage.
150 erent biphasic model systems (linoleic acid; liposome; emulsion) containing myofibrillar protein (MFP
151                                         Nano-liposome encapsulation resulted in a significant reducti
152                                Here we adapt liposome encapsulation to enable the modular, controlled
153 lation, inclusion in emulsions, suspensions, liposomes, etc., that are being employed to maintain sta
154 ding measurements of mixed anionic, cationic liposomes, extracellular vesicles in plasma, and in situ
155                                        Using liposome flotation assays, we demonstrate that an extend
156 cted to targeted lung delivery of EHITSN via liposomes for 20 days.
157  are often superior to detergent micelles or liposomes for membrane protein solubilization.
158  novel method for delivering anti-miRs using liposomes for the functional knockdown of microRNAs.
159 ties and spectral features, in detergent and liposomes, for residues at the pore domain that agree wi
160 sitions and probe the mechanism of templated liposome formation by capturing key intermediates during
161 ceptor, when purified and reconstituted into liposomes, forms an intrinsic dye-permeable pore in the
162           Notably, Siglec-engaging antigenic liposomes formulated with an hCD22 ligand were shown to
163 t change in the PV and zeta potential of the liposome formulations with alpha-tocopherol was observed
164 ave shown that dehydrins are able to protect liposomes from cold damage, but the interactions that dr
165  low-pH-dependent fusion of isolated VLPs to liposomes: fusion pores formed and expanded, as demonstr
166 sing full-length t- and v-SNAREs embedded in liposomes, Gbetagamma inhibited Ca(2+)/synaptotagmin-dep
167 nanoparticles prepared from metallochelation liposomes, His-tagged antigen rOspA from Borrelia burgdo
168 cited via evanescent waves and amplified via liposomes; (ii) the use of two polyclonal antibodies in
169  covalent linkage of well-ordered trimers to liposomes in high-density array displays multiple advant
170       In neutron scattering experiments with liposomes in the presence or absence of Chol, MA prefere
171  Depletion of phagocytic cells by clodronate liposomes in wild-type mice resulted in a reduction of g
172  enhanced retention of exosomes, compared to liposomes, in the circulation of mice is likely due to C
173 9, consisting of dimethyldioctadecylammonium liposomes incorporating two immunomodulators (monomycoly
174 followed the order of emulsion>linoleic acid>liposome, indicating the steric role of proteins.
175  degrees C) was completed within 90min after liposome infusion administered sequentially in three reg
176 uates the penetration of doxorubicin-encased liposomes into three-dimensional cell cultures, or spher
177 endosomal SNARE proteins suffices to convert liposomes into trafficking vesicles that dock and fuse w
178                                Consequently, liposome is an efficient carrier for protection and impr
179                Remote drug loading into nano-liposomes is in most cases the best method for achieving
180  reconstructs of PSI reconstitution in DPhPG liposomes is studied.
181  efficacy of treatment with long-circulating liposomes (LCL) containing prednisolone phosphate (PLP-L
182 s are exploited to prepare biofunctionalized liposome-like nanovesicles (BLNs) that can artificially
183 g nanostructured lipid carrier (NLCs) within liposomes (Lip-NLCs).
184  by fixing the main experimental conditions: liposome lipid composition and size to be similar to tho
185 ra from mice are injected sc with individual liposome-loaded analogues, causing proliferation of bone
186  was applied to improve the effectiveness of liposome loading with essential oils.
187 otoacoustic sensor (LP-hCy7) composed of the liposome (LP) and MeHg(+) -responsive near-infrared (NIR
188 a helianthus, was encapsulated with OVA into liposomes (Lp/OVA/StII) to assess their efficacy to indu
189 osomes (NTSLs) and low temperature sensitive liposomes (LTSLs).
190 otein was functional when reconstituted into liposomes made from yeast total lipid extract.
191 tal studies were carried out in autoxidizing liposome medium by monitoring the development of fluores
192 compounds to inhibit lipid peroxidation in a liposome membrane system was examined by monitoring oxyg
193          The inhibitory effect of ethanol on liposome-membrane fusion is large enough to provide a po
194 hat efficient lipid mixing between viral and liposome membranes requires close to physiological tempe
195 y changes were observed upon AA1 binding for liposomes mimicking mammalian cell membranes, which cons
196                             Supported binary liposome mixture of cationic liposome N-[1-(2,3-Dioleoyl
197  in the DPPH and FRAP assay, although in the liposome model, the guaiacylcatechinpyrylium was more ef
198 upported binary liposome mixture of cationic liposome N-[1-(2,3-Dioleoyloxy)propyl]-N,N,N-trimethylam
199 tumor drug delivery from non-thermosensitive liposomes (NTSLs) and low temperature sensitive liposome
200 etic immunization, previously we showed that liposomes of cationic amphiphiles containing mannose-mim
201 n of 34 nm radius, fluid-phase and gel-phase liposomes onto a titanium oxide-coated surface.
202 mplex with a membrane protein, essential for liposome or nanodiscs reconstitutions.
203  as on its membrane domain, reconstituted in liposomes or in detergent micelles, revealed in all case
204                            Whether formed in liposomes or in mitochondrial outer membranes, Bax-induc
205 itution in artificial lipid bilayers such as liposomes or nanodiscs.
206 iant unilamellar vesicles (GUVs) and smaller liposomes or purified secretory granules with high tempo
207 s combined that are not observed with either liposomes or ubiquitin alone.
208               Using planar lipid bilayer and liposome patch clamp electrophysiology, we show that a s
209 RS enabled to estimate skin concentration of liposomes (percent of injected dose per gram).
210 ctroscopy and in L-alpha-phosphatidylcholine liposome peroxidation assay measured following formation
211 hobic near-infrared (NIR) dye IR780 into the liposome phospholipid bilayer, the bilayer would be disr
212                                         When liposomes poor in sphingomyelin/cholesterol or mimicking
213                                            A liposome pull-down screen identifies KIF5B, the heavy ch
214 on (GLA-SE) or glucopyranosyl lipid adjuvant-liposome-QS21 (GLA-LSQ) adjuvant system significantly in
215               The particle size of the fresh liposomes ranged from 75.7 to 81.0 nm and zeta potential
216 ular and cellular mechanisms responsible for liposome-reconstituted recombinant human WNT3A protein (
217 nable therapeutically viable API-loaded nano-liposomes, referred to as nano-drugs.
218 P, either in solution or bound to artificial liposomes, released BICD2 from an autoinhibited state an
219 ed state of reconstituted KirBac1.1 in giant liposomes, resulting in a higher open probability due to
220 ro-3-phosphocholine (DMPC) and POPC/POPS 3:1 liposomes retain a bilayer macroscopic phase even at the
221 tential measurements of PI(4,5)P2 containing liposomes reveal that Ca(2+) as well as Mg(2+) reduce th
222                       Electron microscopy of liposomes revealed nanometric and spherical-shaped vesic
223               We demonstrate here the use of liposome rupture impact voltammetry for the qualitative
224 reliable detection of viruses by nonfaradaic liposome rupture impact voltammetry with the aid of 1,2-
225  ([S]-HDL), polymeric micelles ([S]-PM), and liposomes ([S]-LIP), that are loaded with the HMG-CoA re
226 efficiency of delivery vesicles, controlling liposome shape (both statically and dynamically) is of u
227 posomes with short-circulating non-PEGylated liposomes showed much higher accumulation of PEGylated l
228 hen non-targeting peptides or siRNA alone or liposome-siRNA alone were used.
229 ferent ratios to generate a small library of liposome-siRNA complexes (lipoplexes) with different phy
230 y, the anchoring of GAD65 to exosome-mimetic liposomes strongly boosted antigen presentation and T-ce
231 s was insensitive to treatment with ceramide liposomes, suggesting specific involvement of ceramide i
232 myristoyl-sn-glycero-3-phosphocholine (DMPC) liposomes, suggesting that lateral gating of the BamA ba
233 water dynamics on different polypeptides and liposome surfaces and find the DW dynamics on globular p
234 aces of proteoliposomes or were spawned from liposome surfaces.
235                                              Liposome suspensions were concentrated by ultracentrifug
236 t detectable in calorimetric measurements on liposome suspensions.
237 than 25% of the ANE initially present in the liposome suspensions.
238                     We created MOM-mimicking liposome systems, which resemble the cellular situation
239 lated and the targeting efficacy of targeted liposomes (t-L) was assessed by cell uptake and cytotoxi
240                                     Targeted liposomes (t-L) were formulated and the targeting effica
241                  Compared with non-targeting liposomes, T7&SHp-P-LPs/ZL006 could transport across BCE
242 ors with the hydrophilic drug into preformed liposome templates.
243 ve pharmaceutical ingredients (API) per nano-liposome that enable therapeutically viable API-loaded n
244          MM-302 is a HER2-targeted PEGylated liposome that encapsulates doxorubicin to facilitate its
245                            We also show that liposomes that contain different cascades can be fused i
246 econd-generation cobalt- and maleimide-based liposomes that have improved in vitro stability over nic
247 showed much higher accumulation of PEGylated liposomes that persisted several days after the liposome
248                                  Compared to liposomes, the engineered exosomes (known as iExosomes)
249     In the absence of ubiquitin or substrate liposomes, the overall structure of the C-terminal domai
250                                         Like liposomes, the vesicle shell is composed of two layers o
251                               However, using liposome titrations under Ca(2+) saturating conditions,
252 ta-potential changed from +3.9mV in uncoated liposomes to +45.5mV in biopolymer-coated liposomes.
253 ergosterol fusion assay to measure fusion of liposomes to a planar lipid bilayer (BLM).
254  well as Mg(2+) reduce the zeta potential of liposomes to nearly background levels of pure phosphatid
255 mg/kg) followed by intravenous DTX (5 mg/kg) liposome treatment revealed regression of xenograft tumo
256 eripheral macrophage depletion by clodronate liposome treatment.
257 ry of Doxorubicin (Dox) with thermosensitive liposomes (TSL) and hyperthermia (HT) has shown preclini
258 red drug delivery from temperature-sensitive liposomes (TSLs), and combinations of the above were inv
259 erefore, we employed these four radiolabeled liposome types as platforms to demonstrate a new concept
260 anol-injection method was applied to prepare liposomes using hydrogenated (Phospholopion-90H and 80H)
261 palmitoyl-sn-glycero-3-phosphocholine (DPPC) liposomes verified that the LSPR measurement discriminat
262 R) during the de novo formation of synthetic liposomes via native chemical ligation.
263 for polymeric and lipid-based nanoparticles, liposomes, virosomes, virus-like particles, dendrimers a
264 and anti-metastasis efficacy of CREKA-loaded liposome was more obvious than that of free Dox or unmod
265                      For these reasons, nano-liposome was used to nano-encapsulate fish oil in this s
266 inclusion complex formation and loading into liposomes was applied to improve the effectiveness of li
267 wed that the maximum loading capacity of the liposomes was around 1.5% of curcumin, although the load
268  decreased when the cholesterol level in the liposomes was close to physiological concentrations.
269                         The particle size of liposomes was in the range of 82.4-107.2nm.
270 ipids on the characteristics of freeze-dried liposomes was investigated using hydroxypropyl-ss-cyclod
271                  The PE encapsulation in the liposomes was responsible for changes in the dynamics of
272 varying lipid acyl chain length in synthetic liposomes we show that BamA has a greater catalytic effe
273                              For comparison, liposomes were also remote-loaded and surface labeled wi
274             Furthermore, hepatocyte-targeted liposomes were developed to deliver the carboxylated der
275                                              Liposomes were eluted out in less than 6 min, about 10 m
276                                The optimized liposomes were further used to achieve efficient and sel
277                              The lyophilized liposomes were incorporated in squid surimi gels at 10.5
278                                              Liposomes were prepared from saturated (Phospholipon 90H
279 reparation, modification and purification of liposomes which offers lab-on-chip scale production.
280 t and chemically specific directed motion of liposomes, which can be exploited in driven processes.
281           One option is encapsulation within liposomes, which enables chemical reactions to proceed i
282 we conclude the successful remote-loading of liposomes with (52)Mn, and furthermore that (52)Mn-DOTA
283 report optimized protocols for radiolabeling liposomes with (52)Mn, through both remote-loading and s
284 dic architectures for the mass production of liposomes with a view to potential industrial translatio
285 the assembly, arrangement and remodelling of liposomes with designer geometry: all of which are exqui
286 l formulations and cells tested, dual-ligand liposomes with equal ligand valencies achieved enhanced
287    Using this method, we produce homogeneous liposomes with four distinct predefined sizes.
288 ng others, are transcribed from DNA cages to liposomes with high fidelity, giving rise to membrane cu
289 Ca(2+)-stimulated fusion of VAMP8-containing liposomes with liposomes containing exocytic or endosoma
290                                              Liposomes with modified lipid head groups have a unique
291 ughput, high-yielding routes to monodisperse liposomes with multiple compartments have not been demon
292  Doxil, Doxil-like liposomes, and Doxil-like liposomes with reduced cholesterol and pegylation.
293 n of DiR labeled, long-circulating PEGylated liposomes with short-circulating non-PEGylated liposomes
294                                              Liposomes with surface-conjugated (52)Mn-DOTA exhibited
295 were encapsulated in soy phosphatidylcholine liposomes with the addition of glycerol.
296                                              Liposomes with the covalently linked EGFR antibody Erbit
297 nstructs and guided the insertion of PR into liposomes with the unoccupied terminal end facing inward
298  the factors affecting the delivery process, liposomes with varying compositions, taken as model synt
299                                    PEGylated liposomes with varying ratios of the targeting peptides
300 sed on the entrapment of phosphatidylcholine liposomes, within a WPC matrix through electrospraying,

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