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
Preparation of Quantum Dot/Drug Nanoparticle Formulations for Traceable Targeted Delivery and Therap
https://www.thno.org/v02p0681.htm
Preparation of Quantum Dot/Drug Nanoparticle Formulations for Traceable Targeted Delivery and Therapy Theranostics 13
Sarcoma-Targeting Peptide-Decorated Polypeptide Nanogel Intracellularly Delivers Shikonin for Upregu
https://www.thno.org/v08p1361.htm
Sarcoma-Targeting Peptide-Decorated Polypeptide Nanogel Intracellularly Delivers Shikonin for Upregulated Osteosarcoma Necroptosis and Diminished
Dual Receptor Recognizing Cell Penetrating Peptide for Selective Targeting, Efficient Intratumoral D
https://www.thno.org/v06p0177.htm
Dual Receptor Recognizing Cell Penetrating Peptide for Selective Targeting, Efficient Intratumoral Diffusion and Synthesized Anti-Glioma Therapy
Tumor-penetrating Peptide Conjugated and Doxorubicin Loaded T1-T2 Dual Mode MRI Contrast Agents Nano
https://www.thno.org/v08p0092.htm
Tumor-penetrating Peptide Conjugated and Doxorubicin Loaded T1-T2 Dual Mode MRI Contrast Agents Nanoparticles for
Cell-penetrating Peptide-modified Targeted Drug-loaded Phase-transformation Lipid Nanoparticles Comb
https://www.thno.org/v08p1892.htm
Cell-penetrating Peptide-modified Targeted Drug-loaded Phase-transformation Lipid Nanoparticles Combined with Low-intensity Focused Ultrasound for
Engineering a spleen-selective mRNA-LNPs vaccine by decoupling the inflammation from cellular immuni
https://www.thno.org/v15p9643.htm
requires APCs expressing antigen proteins and presenting them to T cells via Peptide-MHC Complex (pMHC) effectively
PEG-coated nanoparticles detachable in acidic microenvironments for the tumor-directed delivery of c
https://www.thno.org/v10p6695.htm
N peptide to NG2 receptor, leading to effective antiangiogenic therapy [ 25 ]. C peptide displays high potency and
Developing an efficient MGCR microneedle nanovaccine patch for eliciting Th 1 cellular response agai
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
iRGD-TRP-PK1-modified red blood cell membrane vesicles as a new chemotherapeutic drug delivery and t
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
Strategy to enhance lung cancer treatment by five essential elements: inhalation delivery, nanotechn
https://www.thno.org/v09p8362.htm
anticancer drug, inhibitors of different types of EGFR-TKs and peptide targeted to the
Supramolecular nanofibers co-loaded with dabrafenib and doxorubicin for targeted and synergistic the
https://www.thno.org/v13p2140.htm
potential approach for DTC treatment. In this study, a supramolecular peptide nanofiber (SPNs) co-loaded
Lymph node-targeting adjuvant/neoantigen-codelivering vaccines for combination glioblastoma radioimm
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
A carrier-free long-acting ropivacaine formulation using methylprednisolone sodium succinate as a du
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
Alliance with EPR Effect: Combined Strategies to Improve the EPR Effect in the Tumor Microenvironmen
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
Nanodefensin-encased hydrogel with dual bactericidal and pro-regenerative functions for advanced wou
https://www.thno.org/v11p3642.htm
owing to their poor pharmacological properties and lack of suitable pharmaceutical formulations. Nanodefensin (ND), a
Rational design of Polymeric Hybrid Micelles to Overcome Lymphatic and Intracellular Delivery Barrie
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
Platinum-Based Nanovectors Engineered with Immuno-Modulating Adjuvant for Inhibiting Tumor growth an
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
Redox dyshomeostasis modulation of the tumor intracellular environment through a metabolic intervent
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
Superparamagnetic Iron Oxide Nanoparticles as MRI contrast agents for Non-invasive Stem Cell Labelin
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
Targeting DAD1 gene with CRISPR-Cas9 system transmucosally delivered by fluorinated polylysine nanop
https://www.thno.org/v14p0203.htm
ε-Poly-L-lysine), an antibacterial agent approved by FDA, is a naturally occurring peptide and biodegradable
Mannosylated Lipid Nano-emulsions Loaded with Lycorine-oleic Acid Ionic Complex for Tumor Cell-speci
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
Transformable prodrug nanoplatform via tumor microenvironment modulation and immune checkpoint block
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
Phase-Change Nanoparticles Using Highly Volatile Perfluorocarbons: Toward a Platform for Extravascul
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
Nano-delivery of fraxinellone remodels tumor microenvironment and facilitates therapeutic vaccinatio
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
Combined delivery of sorafenib and a MEK inhibitor using CXCR4-targeted nanoparticles reduces hepati
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
Proinflammatory macrophage-derived microvesicles exhibit tumor tropism dependent on CCL2/CCR2 signal
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
A general strategy towards activatable nanophotosensitizer for phototoxicity-free photodynamic thera
https://www.thno.org/v15p0943.htm
phthalocyanine, ZnPc) as proof of concept and incorporating the cRGD peptide via a multi
One-pot synthesis of a microporous organosilica-coated cisplatin nanoplatform for HIF-1-targeted com
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
Tumor-responsive cuproptosis nanoinducer realizing efficient PANoptosis for enhanced cancer immunoth
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
Polymeric microneedles enable simultaneous delivery of cancer immunomodulatory drugs and detection o
https://www.thno.org/v13p0001.htm
acids) either in the form of free drugs or as nano-formulations [ 3 , 4 ]. Applying these
A Nanosystem of Amphiphilic Oligopeptide-Drug Conjugate Actualizing Both αvβ3 Targeting and Reductio
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
Site-specific albumin tagging with NIR-II fluorogenic dye for high-performance and super-stable bioi
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
Oxidative stress-mediated PANoptosis and ferroptosis: Exploration of multimodal cell death triggered
https://www.thno.org/v15p6665.htm
within DSPE-PEG 2000 and functionalizing it with TAT (a cell-penetrating peptide) to enhance
Self-assembly of nanomicelles with rationally designed multifunctional building blocks for synergist
https://www.thno.org/v12p2028.htm
9 in MDA-MB-231 cells were assessed based on the specific protease-peptide substrate chromogenic reaction. In
Co-delivery of VEGF siRNA and Etoposide for Enhanced Anti-angiogenesis and Anti-proliferation Effect
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
Enhanced Therapeutic Effect of RGD-Modified Polymeric Micelles Loaded With Low-Dose Methotrexate and
https://www.thno.org/v09p0708.htm
an essential role in the progression of rheumatoid arthritis (RA). RGD peptide shows high affinity and
Aristolochic acid mutational signature defines the low-risk subtype in upper tract urothelial carcin
https://www.thno.org/v10p4323.htm
the AA mutational signature with the consumption of AA-containing herbal formulations. Fifty-nine percent of
A novel Granzyme B nanoparticle delivery system simulates immune cell functions for suppression of s
https://www.thno.org/v09p7616.htm
granzyme B protein within a porous polymeric nanocapsule. Methods : A cell-penetrating peptide TAT was attached onto
GRP78-targeted ferritin nanocaged ultra-high dose of doxorubicin for hepatocellular carcinoma therap
https://www.thno.org/v09p2167.htm
Fan 1 , Xiyun Yan 1,2 1. Key Laboratory of Protein and Peptide Pharmaceuticals, CAS-University of
Platelet-camouflaged nanococktail: Simultaneous inhibition of drug-resistant tumor growth and metast
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
Molecular Imaging of Stem Cells: Tracking Survival, Biodistribution, Tumorigenicity, and Immunogenic
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
A New Concept of Enhancing Immuno-Chemotherapeutic Effects Against B16F10 Tumor via Systemic Adminis
https://www.thno.org/v06p2141.htm
successfully design a paclitaxel (PTX) and alpha-galactosylceramide (αGC) co-loaded TH peptide (AGYLLGHINLHHLAHL(Aib)HHIL-Cys
Albumin-seeking dyes with adjustable assemblies in situ enable programmable imaging windows and targ
https://www.thno.org/v14p2675.htm
reactions and potentially limiting the repeated administration of PEG-containing formulations. The other
Scavenger Receptor B1 is a Potential Biomarker of Human Nasopharyngeal Carcinoma and Its Growth is I
https://www.thno.org/v03p0477.htm
examined the SR-B1 targeting ability of a highly biocompatible HDL-mimicking peptide-phospholipid scaffold (HPPS) nanocarrier
Ion drugs for precise orthotopic tumor management by in situ the generation of toxic ion and drug po
https://www.thno.org/v12p0734.htm
B) Tumor growth curves of U87MG tumor-bearing mice exposed to different formulations after the 21
An In Vivo Evaluation of the Effect of Repeated Administration and Clearance of Targeted Contrast Ag
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
High-Yield Synthesis of Monomeric LMWP(CPP)-siRNA Covalent Conjugate for Effective Cytosolic Deliver
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
ICAM-1-Targeted, Lcn2 siRNA-Encapsulating Liposomes are Potent Anti-angiogenic Agents for Triple Neg
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
GSH-sensitive Pt(IV) prodrug-loaded phase-transitional nanoparticles with a hybrid lipid-polymer she
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
Nanotheranostics ˗ Application and Further Development of Nanomedicine Strategies for Advanced Thera
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
Low Molecular Weight Heparin-Coated and Dendrimer-Based Core-Shell Nanoplatform with Enhanced Immune
https://www.thno.org/v09p0337.htm
on cell migration and invasion The inhibitory effects of different formulations on the migration
Self-Assembly of Gold Nanoparticles Shows Microenvironment-Mediated Dynamic Switching and Enhanced B
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
Combination therapy with ropivacaine-loaded liposomes and nutrient deprivation for simultaneous canc
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
Recent advances and challenges in hydrogel-based delivery of immunomodulatory strategies for diabeti
https://www.thno.org/v16p0516.htm
α and IL-1β); Promoting angiogenesis and collagen deposition 14 days [ 72 ] hUCMSCs Peptide RADA16-I; Peptide KLT
Dual-pH Sensitive Charge-reversal Nanocomplex for Tumor-targeted Drug Delivery with Enhanced Antican
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
Sustained Release of Immunosuppressant by Nanoparticle-anchoring Hydrogel Scaffold Improved the Surv
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
Dual-Energy CT Imaging of Tumor Liposome Delivery After Gold Nanoparticle-Augmented Radiation Therap
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
Intelligent gold nanostars for in vivo CT imaging and catalase-enhanced synergistic photodynamic & p
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
Investigation of In Vivo Targeting Kinetics of αvβ3-Specific Superparamagnetic Nanoprobes by Time-Re
https://www.thno.org/v01p0263.htm
expression in resting endothelium. Using nanoprobes conjugated with a cyclic RGDfK (cRGD) peptide, an α v β
Ultrasound-mediated cavitation enhances the delivery of an EGFR-targeting liposomal formulation desi
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
Cooperation of endogenous and exogenous reactive oxygen species induced by zinc peroxide nanoparticl
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