JamBot Logo
1-100 of about 126 matches for site:www.thno.org peptide formulations
https://www.thno.org/v09p7807
elucidating the impacts of peptide length and formulations on their immunogenicity, peptide-based immunomodulating agents can
https://www.thno.org/v09p7807.htm
elucidating the impacts of peptide length and formulations on their immunogenicity, peptide-based immunomodulating agents can
https://www.thno.org/v14p2290.htm
and long neoantigen peptides (antigen peptide from ovalbumin: OVA 257-264 , and neoantigen peptide in MC
https://www.thno.org/v02p0681.htm
Preparation of Quantum Dot/Drug Nanoparticle Formulations for Traceable Targeted Delivery and Therapy Theranostics   13
https://www.thno.org/v08p1361.htm
Sarcoma-Targeting Peptide-Decorated Polypeptide Nanogel Intracellularly Delivers Shikonin for Upregulated Osteosarcoma Necroptosis and Diminished
https://www.thno.org/v06p0177.htm
Dual Receptor Recognizing Cell Penetrating Peptide for Selective Targeting, Efficient Intratumoral Diffusion and Synthesized Anti-Glioma Therapy
https://www.thno.org/v08p0092.htm
Tumor-penetrating Peptide Conjugated and Doxorubicin Loaded T1-T2 Dual Mode MRI Contrast Agents Nanoparticles for
https://www.thno.org/v08p1892.htm
Cell-penetrating Peptide-modified Targeted Drug-loaded Phase-transformation Lipid Nanoparticles Combined with Low-intensity Focused Ultrasound for
https://www.thno.org/v15p9643.htm
requires APCs expressing antigen proteins and presenting them to T cells via Peptide-MHC Complex (pMHC) effectively
https://www.thno.org/v10p6695.htm
N peptide to NG2 receptor, leading to effective antiangiogenic therapy [ 25 ]. C peptide displays high potency and
https://www.thno.org/v13p4821.htm
antibody response with 2.14-fold higher IgG titer than Alum adjuvant vaccine. The peptide pools assay demonstrated the
https://www.thno.org/v15p0086.htm
treatment with different formulations. (C) Statistical analysis of tumor volume after treatment with different formulations. (D) Representative images of
https://www.thno.org/v09p8362.htm
anticancer drug, inhibitors of different types of EGFR-TKs and peptide targeted to the
https://www.thno.org/v13p2140.htm
potential approach for DTC treatment. In this study, a supramolecular peptide nanofiber (SPNs) co-loaded
https://www.thno.org/v13p4304.htm
elicit anti-cancer adaptive immunity, which can be synergistically combined with ICB and radiotherapy. Peptide vaccines are attractive for
https://www.thno.org/v15p3862.htm
been a promising strategy for pursuing long-acting opioid-free analgesia. Although many formulations based on carrier materials
https://www.thno.org/v02p1117.htm
Herein, we review recent development of nanotheranostics using lipid- and polymer-based formulations, with a particular
https://www.thno.org/v13p1520.htm
variety of materials have been designed to target PD-L1, including antibodies, nanoparticle, peptide, aptamer, RNA, and
https://www.thno.org/v09p8073.htm
4T1 [ 42 ] ECM EGFR HA Dual-targeting strategy with low toxicity HCCLM3 [ 44 ] Enzyme Cathepsin B Peptide (FRRG) Self-assembling carrier
https://www.thno.org/v11p3642.htm
owing to their poor pharmacological properties and lack of suitable pharmaceutical formulations. Nanodefensin (ND), a
https://www.thno.org/v07p4383.htm
of cationic PCL-PEI were prepared and loaded with tyrosinase-related protein 2 (Trp2) peptide and adjuvant
https://www.thno.org/v10p0657.htm
and efficiency in activating immune responses. Methods : We synthesized a self-assembling peptide (Fbp-G D F
https://www.thno.org/v09p8018.htm
research has yielded early-stage clinical products as exemplified by the FDA-approved nano formulations (Abraxane ® for paclitaxel
https://www.thno.org/v09p7826.htm
to LPS and has been employed in some clinically explored vaccine formulations [ 19 - 21 ]. Although LPS
https://www.thno.org/v02p1092.htm
and incubated at 60 o C for 2 h. Commonly, the liposome formulations were stored at 4
https://www.thno.org/v08p2974.htm
polymeric core and conjugated with platinum-based compounds as therapeutics and WKYMVm peptide (Wpep) as a
https://www.thno.org/v02p0714.htm
yielded a size of <50 nm for the micellar formulations with very narrow size
https://www.thno.org/v08p2782.htm
with his-tagged C-terminus fragment (50-200 g/mL, 100 s). Subsequently, association with No peptide, negative control peptide (NCP
https://www.thno.org/v02p0695.htm
pharmacokinetics and biodistribution. In this report, we have developed quantum rod (QR) based formulations for the
https://www.thno.org/v12p6143.htm
were further functionalized with a lipid bilayer consisting of the RGD peptide using a simple
https://www.thno.org/v06p1336.htm
drug delivery applications and have led to several clinically approved therapeutic drug formulations, including Caelyx, Myocet, and
https://www.thno.org/v03p0595.htm
DTPA bearing poly(ethyleneimine) (SiO 2 /Gd-DTPA-PEI) [ 31 ] and Gd 3+ conjugated peptide dendrimers [ 37 - 39 ] provide
https://www.thno.org/v13p5305.htm
loaded with the cRGD-PP as a co-delivery nano-system. Different formulations were injected into mice
https://www.thno.org/v09p3388.htm
reagents and solvents were obtained from commercial sources without further purification. Preparation of peptide derivates Peptide derivates of
https://www.thno.org/v10p7403.htm
serve as either active agents or formulation supplements. In terms of drug formulations and delivery
https://www.thno.org/v14p0203.htm
ε-Poly-L-lysine), an antibacterial agent approved by FDA, is a naturally occurring peptide and biodegradable
https://www.thno.org/v02p1104.htm
8±4.3 0.156±0.019 82.7±1.6% Intracellular distribution of formulations The intracellular
https://www.thno.org/v02p0723.htm
The release profile was monitored for over 10 days. It was observed that both formulations show sustained release of
https://www.thno.org/v13p1906.htm
and reduction dual-responsive polymersomal prodrug (TRPP) nanoplatform was constructed when the D-peptide antagonist ( D PPA-1
https://www.thno.org/v15p6184.htm
for intelligent keloid therapy. The UCNPs were functionalized by the ferritin homing peptide (HKN 15 ) and
https://www.thno.org/v02p1185.htm
restrict the particles to flow only through the vascular networks. Formulations of MCAs
https://www.thno.org/v08p4884.htm
drug, thus contributing to improved anti-cancer efficacy. Endowed with TNBC-targeting ligand uPA peptide, uPA-PTXD NPs exhibited
https://www.thno.org/v08p3781.htm
100 μg/mice) and Frax NE combined with BRAF peptide vaccine group (Combo). BRAF peptide vaccine was prepared as
https://www.thno.org/v08p0894.htm
Taoyuan, Taiwan). Tris(2-carboxyethyl)phosphine (TCEP) disulfide reducing gels were purchased from Thermo Fisher. CTCE9908 peptide (sequence: Lys-Gly-Val
https://www.thno.org/v10p10513.htm
and various versatile nanocarriers such as polymeric nanoparticles [ 13 , 14 ], micelles [ 15 , 16 ], liposomes [ 17 ], peptide-based nanoparticles [ 18 , 19
https://www.thno.org/v10p6581.htm
23 ]. The protein concentration was quantified using the BCA kit. The peptide samples were desalted and
https://www.thno.org/v02p0045.htm
is possible to conjugate a targeting motif, such as a peptide [ 40 , 41 ] or an
https://www.thno.org/v15p0943.htm
phthalocyanine, ZnPc) as proof of concept and incorporating the cRGD peptide via a multi
https://www.thno.org/v10p2918.htm
and select import option Reference Manager (RIS). Click on Import. File import instruction Abstract Nanoparticle formulations have proven effective for
https://www.thno.org/v15p9294.htm
The co-administration of cell death inducers as simple mixture of soluble formulations cannot guarantee expected therapeutical
https://www.thno.org/v09p1893.htm
targeting tumor angiogenic vessels and cells along with EPR effect. We have prepared RGD peptide-conjugated and αvβ3
https://www.thno.org/v13p0001.htm
acids) either in the form of free drugs or as nano-formulations [ 3 , 4 ]. Applying these
https://www.thno.org/v07p3306.htm
strategy and the synergistic effect between them, we synthesized four small molecule amphiphilic peptide-drug conjugates (APDCs) using
https://www.thno.org/v03p0865.htm
predictive for myocardial salvage after myocardial infarction [ 102 ]. Targeting monocytes has been performed using various formulations of superparamagentic
https://www.thno.org/v14p1860.htm
2797 m/z) using Byonic. The full mass (MS1) of the peptide was calculated to
https://www.thno.org/v03p0201.htm
Transfection was performed as described above, but with Atto 647N labeled siRNA for all formulations. Cells were incubated overnight
https://www.thno.org/v09p5797.htm
in avidity [ 23 ]. Langerin and DC-SIGN appear to require different formulations to meet
https://www.thno.org/v15p6665.htm
within DSPE-PEG 2000 and functionalizing it with TAT (a cell-penetrating peptide) to enhance
https://www.thno.org/v12p2028.htm
9 in MDA-MB-231 cells were assessed based on the specific protease-peptide substrate chromogenic reaction. In
https://www.thno.org/v09p5886.htm
every other day; (D) Representative H&E images of orthotopic A549 lung tumors after different formulations treatment. Different formulations represented
https://www.thno.org/v09p0708.htm
an essential role in the progression of rheumatoid arthritis (RA). RGD peptide shows high affinity and
https://www.thno.org/v10p4323.htm
the AA mutational signature with the consumption of AA-containing herbal formulations. Fifty-nine percent of
https://www.thno.org/v09p7616.htm
granzyme B protein within a porous polymeric nanocapsule. Methods : A cell-penetrating peptide TAT was attached onto
https://www.thno.org/v09p2167.htm
Fan 1 , Xiyun Yan 1,2 1. Key Laboratory of Protein and Peptide Pharmaceuticals, CAS-University of
https://www.thno.org/v08p2683.htm
MNPs/DOX was developed by encapsulating melanin nanoparticles (MNPs) and doxorubicin (DOX) inside RGD peptide (c(RGDyC))-modified nanoscale
https://www.thno.org/v02p0335.htm
can induce changes in T2 relaxivity at nanomolar concentrations [ 12 ], and many formulations are FDA-approved for
https://www.thno.org/v05p0746.htm
other combinations of PEG, including peptide-PEG 2000 /PEG 2000 liposomes and peptide-PEG 350 /PEG 2000
https://www.thno.org/v06p2141.htm
successfully design a paclitaxel (PTX) and alpha-galactosylceramide (αGC) co-loaded TH peptide (AGYLLGHINLHHLAHL(Aib)HHIL-Cys
https://www.thno.org/v14p2675.htm
reactions and potentially limiting the repeated administration of PEG-containing formulations. The other
https://www.thno.org/v03p0477.htm
examined the SR-B1 targeting ability of a highly biocompatible HDL-mimicking peptide-phospholipid scaffold (HPPS) nanocarrier
https://www.thno.org/v12p0734.htm
B) Tumor growth curves of U87MG tumor-bearing mice exposed to different formulations after the 21
https://www.thno.org/v03p0093.htm
single imaging study to evaluate short-term biological changes, system parameters, or novel microbubble formulations [ 9 , 10 , 11 , 12
https://www.thno.org/v07p2495.htm
of this coupling technique is significant, far-reaching and wide-spread. Keywords : cell penetrating peptide, siRNA delivery, covalent CPP
https://www.thno.org/v12p1756.htm
size-shrinkable nanoparticles, “cluster bomb”-like sequential-releasing nanoparticles, charge-reversal nanoparticles, and penetrating peptide-modified nanoparticles [ 27 ]. For
https://www.thno.org/v06p0001.htm
group presented on the ICAM-1 antibody or the IgG. Three liposome formulations were tested for
https://www.thno.org/v08p2765.htm
that selectively binds to CSA [ 17 ]; we named this synthetic peptide placental CSA binding peptide (plCSA-BP). Given this
https://www.thno.org/v09p1047.htm
DSPE-PEG 1k -Pt(IV), and an active targeting ligand, the cRGD peptide (PLGA: poly(lactic-co
https://www.thno.org/v06p1274.htm
medicine [ 3 ]. Then, Lu and his team specified recent developments in liposomal formulations for disease
https://www.thno.org/v04p0660.htm
Delivery of single theranostic agent [ 108 ] Gold nanoparticles Gold nanoparticles DOX Gold nanoparticles ~ 55nm CPLGLAGG peptide Stimulus responsive drug release
https://www.thno.org/v07p3856.htm
nanoparticles [ 36 ] and multi-drug loaded 'triolimus' micelles [ 37 ]. Compared to these formulations, the carriers
https://www.thno.org/v09p0337.htm
on cell migration and invasion The inhibitory effects of different formulations on the migration
https://www.thno.org/v07p1875.htm
for brain tumor treatment. However, the clinical applications of the inorganic formulations are often hindered by
https://www.thno.org/v06p0918.htm
address the growing desire for this dual-purpose paradigm, and nanoparticle formulations have recently come to
https://www.thno.org/v10p4885.htm
and DSPE-PEG2000-RGD (Figure 2 A). RGD is a short peptide that is commonly used
https://www.thno.org/v02p0541.htm
sized subcutaneous implant prepared with the copolymer polylactide-co-glycolide (PLGA). Nowadays other protein formulations have come on the
https://www.thno.org/v16p0516.htm
α and IL-1β); Promoting angiogenesis and collagen deposition 14 days [ 72 ] hUCMSCs Peptide RADA16-I; Peptide KLT
https://www.thno.org/v07p1806.htm
nonspecific distribution [ 25 , 26 ]. Cell-penetrating peptides (CPPs), such as transactivator of transcription (TAT) peptide, were able to
https://www.thno.org/v07p1062.htm
between the thiol group of the cysteine in the peptide and the
https://www.thno.org/v06p1528.htm
The abdomen was depilated with depilatory cream one day before administration to facilitate observation. Formulations were administered to
https://www.thno.org/v08p0878.htm
lactic-co-glycolic acid) (PLGA) nanoparticles were modified with RADA16 (RNPs), a self-assembling peptide, and then
https://www.thno.org/v11p9833.htm
in the blood long circulation [ 33 ] whereas the luteinizing hormone-releasing hormone (LHRH) peptide and hyaluronic
https://www.thno.org/v08p1782.htm
used ligands for targeting tumor epithelium is the RGD (Arg-Gly-Asp) peptide, which has high affinity
https://www.thno.org/v03p0496.htm
compared to targeting the tumor cells alone. For example, disulfide cyclized peptide derived from the
https://www.thno.org/v09p5424.htm
blood [ 9 ] while simultaneously improving their phototherapeutic activity. However, it has been reported that although nano-formulations can increase the
https://www.thno.org/v03p0099.htm
by a polymer coating technique and coupled with cyclic Arg-Gly-Asp peptide (cRGD) peptides. After confirmation
https://www.thno.org/v01p0263.htm
expression in resting endothelium. Using nanoprobes conjugated with a cyclic RGDfK (cRGD) peptide, an α v β
https://www.thno.org/v09p5595.htm
fractions was measured using an automated Wizard gamma counter. Cellular uptake of fluorescently labelled formulations Rhodamine-containing EGF-LP
https://www.thno.org/v06p1306.htm
a prolonged period with high controllability. Drug delivery refers to the approaches, formulations, technologies, and systems
https://www.thno.org/v09p7200.htm
vivo tumor growth inhibition Mice bearing U87MG tumors (~50 mm 3 ) were injected intravenously with different formulations every other day for
https://www.thno.org/v09p3825.htm
the anticancer activity of GNCs-based drug delivery systems. Methods : pH low insertion peptide (pHLIP)- and thermoresponsive