Browse result page of TopicalPdb


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ID1001SequenceACSSSPSKHCGNameTD1Nature of peptide or cargoTD1 enhances the transdermal delivery of macromoleculesAssayFranz diffusion cellsTissue permeabilitySignificant increase in permeability of the peptide can be seen by the addition of ATP.The amount of protein that permeated the skin was determined with ELISATissue SampleMale SD rats skin cellsPUBMED ID25269793
ID1002SequenceAAPVNameAAPVNature of peptide or cargoIt fits the P-P1 subsites of elastase and inhibits HNE competitivelyAssayFranz diffusion cell, HPLCTissue permeabilityEpidermal flux=0.46 μg/cm2/h, Permeability coefficient=1.50×10−4Kp(cm/h)Tissue SampleHuman epidermal membranes were obtained by heat separation of whole skinPUBMED ID24842663
ID1003SequenceAAPVNameC6(D)-Laa-AAPVNature of peptide or cargoIt fits the P-P1 subsites of elastase and inhibits HNE competitivelyAssayFranz diffusion cell, HPLCTissue permeabilityEpidermal flux=2.29 μg/cm2/h, Permeability coefficient=7.6×10−4 Kp(cm/h)Tissue SampleHuman epidermal membranes were obtained by heat separation of whole skinPUBMED ID24842663
ID1004SequenceAAPVNameC6(L)-Laa- AAPVNature of peptide or cargoIt fits the P-P1 subsites of elastase and inhibits HNE competitivelyAssayFranz diffusion cell, HPLCTissue permeabilityEpidermal flux=0.50 μg/cm2/h, Permeability coefficient=1.6×10−4 Kp(cm/h)Tissue SampleHuman epidermal membranes were obtained by heat separation of whole skinPUBMED ID24842663
ID1005SequenceAAPVNameC8(D,L)-Laa-AAPVNature of peptide or cargoIt fits the P-P1 subsites of elastase and inhibits HNE competitivelyAssayFranz diffusion cell, HPLCTissue permeabilityEpidermal flux=10.08 μg/cm2/h, Permeability coefficient= 3.3×10−3 Kp(cm/h)Tissue SampleHuman epidermal membranes were obtained by heat separation of whole skinPUBMED ID24842663
ID1006SequenceAAPVNameC8(D)-Laa-AAPVNature of peptide or cargoIt fits the P-P1 subsites of elastase and inhibits HNE competitivelyAssayFranz diffusion cell, HPLCTissue permeabilityEpidermal flux=7.42 μg/cm2/h, Permeability coefficient=1.90×10−2 Kp(cm/h)Tissue SampleHuman epidermal membranes were obtained by heat separation of whole skinPUBMED ID24842663
ID1007SequenceAAPVNameC8(L)-Laa-AAPVNature of peptide or cargoIt fits the P-P1 subsites of elastase and inhibits HNE competitivelyAssayFranz diffusion cell, HPLCTissue permeabilityEpidermal flux=1.37 μg/cm2/h, Permeability coefficient=4.50×10−4 Kp(cm/h)Tissue SampleHuman epidermal membranes were obtained by heat separation of whole skinPUBMED ID24842663
ID1008SequenceAAPVNameC10(D,L)-Laa-AAPVNature of peptide or cargoIt fits the P-P1 subsites of elastase and inhibits HNE competitivelyAssayFranz diffusion cell, HPLCTissue permeabilityEpidermal flux=8.92 μg/cm2/h, Permeability coefficient=2.9×10−3 Kp(cm/h)Tissue SampleHuman epidermal membranes were obtained by heat separation of whole skinPUBMED ID24842663
ID1009SequenceRRRRRRRRRRRLILV
LLAI
Name11R-No. 10Nature of peptide or cargoMelanogenesis inhibitory peptideAssayConfocal microscopeTissue permeabilityWhen TMR-11R was topically applied for 24 h, the signals were only observed on the surface of the skin. In contrast, 12 h later, strong signals were detected showing that TMR-11R had arrived at the skin basal layer. Moreover, 24 and 48 hours later, the signals had spread out more and were stronger in both epidermis and dermisTissue SampleSkin from the back of a brown guinea pigPUBMED ID24602570
ID1010SequenceGKRRNameR4 (arginine-terminated peptide dendrimers)Nature of peptide or cargoPeptide dendrimers are wedge-like molecules comprising an amino acid branching core that is most typically decorated with various basic amino acids (e.g. Lys, His, Arg) on their head groupsAssayFranz diffusion cellTissue permeabilityFlux (mg/cm2/h) 25.16 ± 2.31 , Q48 (mg) 1167.05 ± 50.10 Drug content in skin (mg/cm2) 146 ± 6.44 Tissue SampleHuman epidermal skinPUBMED ID24134794
ID1011SequenceGKRRNameR4 (arginine-terminated peptide dendrimers)Nature of peptide or cargoPeptide dendrimers are wedge-like molecules comprising an amino acid branching core that is most typically decorated with various basic amino acids (e.g. Lys, His, Arg) on their head groupsAssayFranz diffusion cellTissue permeabilityFlux (mg/cm2/h) 43.74 ± 4.15 , Q48(mg) 2064.72 ± 100.05 Drug content in skin (mg/cm2) 180 ± 8.23Tissue SampleHuman epidermal skinPUBMED ID24134794
ID1012SequenceGKRRNameR4 (arginine-terminated peptide dendrimers)Nature of peptide or cargoPeptide dendrimers are wedge-like molecules comprising an amino acid branching core that is most typically decorated with various basic amino acids (e.g. Lys, His, Arg) on their head groupsAssayFranz diffusion cellTissue permeabilityFlux (mg/cm2/h) 57.66 ± 4.83 , Q48(mg) 2706.53 ± 123.60, Drug content in skin (mg/cm2) 204 ± 8.41 Tissue SampleHuman epidermal skinPUBMED ID24134794
ID1013SequenceGKKKRRRRNameR8 (arginine-terminated peptide dendrimers)Nature of peptide or cargoPeptide dendrimers are wedge-like molecules comprising an amino acid branching core that is most typically decorated with various basic amino acids (e.g. Lys, His, Arg) on their head groupsAssayFranz diffusion cellTissue permeabilityFlux (mg/cm2/h) ± 4.83 , Q48(mg) 2706.53 ± 123.60, Drug content in skin (mg/cm2) 204 ± 8.41 Tissue SampleHuman epidermal skinPUBMED ID24134794
ID1014SequenceGKKKRRRRNameR8 (arginine-terminated peptide dendrimers)Nature of peptide or cargoPeptide dendrimers are wedge-like molecules comprising an amino acid branching core that is most typically decorated with various basic amino acids (e.g. Lys, His, Arg) on their head groupsAssayFranz diffusion cellTissue permeabilityFlux (mg/cm2/h) 57.66 ± 4.83 , Q48(mg) 2706.53 ± 123.60, Drug content in skin (mg/cm2) 204 ± 8.41 Tissue SampleHuman epidermal skinPUBMED ID24134794
ID1015SequenceGKKKRRRRNameR8 (arginine-terminated peptide dendrimers)Nature of peptide or cargoPeptide dendrimers are wedge-like molecules comprising an amino acid branching core that is most typically decorated with various basic amino acids (e.g. Lys, His, Arg) on their head groupsAssayFranz diffusion cellTissue permeabilityFlux (mg/cm2/h) 78.07 ± 7.52, Q48 (mg) 3666.44 ± 162.70 Drug content in skin (mg/cm2) 378± 15.11Tissue SampleHuman epidermal skinPUBMED ID24134794
ID1016SequenceGKKKKKKKRRRRRRRRNameR16 (arginine-terminated peptide dendrimers)Nature of peptide or cargoPeptide dendrimers are wedge-like molecules comprising an amino acid branching core that is most typically decorated with various basic amino acids (e.g. Lys, His, Arg) on their head groupsAssayFranz diffusion cellTissue permeabilityFlux (mg/cm2/h) 21.43 ± 1.32 , Q48 (mg) 856.29 ± 39.50 Drug content in skin (mg/cm2) 151 ± 4.64 Tissue SampleHuman epidermal skinPUBMED ID24134794
ID1017SequenceGKKKKKKKRRRRRRRRNameR16 (arginine-terminated peptide dendrimers)Nature of peptide or cargoPeptide dendrimers are wedge-like molecules comprising an amino acid branching core that is most typically decorated with various basic amino acids (e.g. Lys, His, Arg) on their head groupsAssayFranz diffusion cellTissue permeabilityFlux (mg/cm2/h) 23.46 ± 2.04 , Q48 (mg) 1106.03 ± 53.80 Drug content in skin (mg/cm2) 155 ± 4.85 Tissue SampleHuman epidermal skinPUBMED ID24134794
ID1018SequenceGKKKKKKKRRRRRRRRNameR16 (arginine-terminated peptide dendrimers)Nature of peptide or cargoPeptide dendrimers are wedge-like molecules comprising an amino acid branching core that is most typically decorated with various basic amino acids (e.g. Lys, His, Arg) on their head groupsAssayFranz diffusion cellTissue permeabilityFlux (mg/cm2/h) 27.16 ± 2.65, Q48 (mg) 1256.61 ± 55.70, Drug content in skin (mg/cm2) 156 ± 6.26 Tissue SampleHuman epidermal skinPUBMED ID24134794
ID1019SequenceKETWWETWWTEWSQP
KKKRKV
NamePep-1Nature of peptide or cargoCell penetrating peptideAssayIn vivo imagingTissue permeabilitySignificant permeability of the peptide can be seen in in vivo imagesTissue SampleMouse skin cellsPUBMED ID23601371
ID1020SequenceACSSSPSKHCGNameTDNNature of peptide or cargoTD-1 has been testified to enhanced insulin transdermal delivery through hair folliclesAssayConfocal Laser Scanning MicroscopyTissue permeabilitySignificant permeability of the peptide can be seen in confocal imagesTissue SampleMale SD rats skin cellsPUBMED ID23391375
ID1021SequenceACSSKKSKHCGNameTD-34Nature of peptide or cargoTD-1 has been testified to enhanced insulin transdermal delivery through hair folliclesAssayConfocal Laser Scanning MicroscopyTissue permeabilitySignificant permeability of the peptide can be seen in confocal imagesTissue SampleMale SD rats skin cellsPUBMED ID23391375
ID1022SequenceACSSSPSKHCGNameTD1Nature of peptide or cargoTD1 enhances the transdermal delivery of macromoleculesAssayFranz diffusion cells, immunity fluorescence techniquesTissue permeabilitySignificant permeability of the peptide can be seen. The amount of protein that permeated the skin was determined with immunity fluorescence techniquesTissue SampleMale SD rats skin cellsPUBMED ID23385091
ID1023SequenceGRKKRRQRRRPPQRKCNameTatNature of peptide or cargoCell penetrating peptideAssayVertical Franz diffusion cellTissue permeabilityTP could not pass through the skin due to the charge repulsion effect between the negative charge of the TP and the negative charge of the skinTissue SampleAbdominal skin of Sprague–Dawley ratsPUBMED ID23311648
ID1024SequenceGRKKRRQRRRPPQRKCNameTatNature of peptide or cargoCell penetrating peptideAssayVertical Franz diffusion cellTissue permeabilityCumulative amounts0.10± 0.01 µg/cm2 and fluxes 0.60 ± 0.06 µg/cm2·hTissue SampleAcceptor compartment of Franz diffusion cell/Abdominal skin of Sprague–Dawley ratsPUBMED ID23311648
ID1025SequenceGRKKRRQRRRPPQRKCNameTatNature of peptide or cargoCell penetrating peptideAssayVertical Franz diffusion cellTissue permeabilityCumulative amounts 0.31 ± 0.04 µg/cm2 and fluxes 1.86 ± 0.24 µg/cm2·hTissue SampleAbdominal skin of Sprague–Dawley ratsPUBMED ID23311648
ID1026SequenceGRKKRRQRRRPPQRKCNameTatNature of peptide or cargoCell penetrating peptideAssayVertical Franz diffusion cellTissue permeabilityCumulative amounts 1.02 ± 0.05 µg/cm2 and fluxes 6.13± 0.28 µg/cm2·hTissue SampleAcceptor compartment of Franz diffusion cell/Abdominal skin of Sprague–Dawley ratsPUBMED ID23311648
ID1027SequenceGRKKRRQRRRPPQRKCNameTatNature of peptide or cargoCell penetrating peptideAssayVertical Franz diffusion cellTissue permeabilityCumulative amounts 4.29 ± 0.40 µg/cm2 and fluxes 25.73 ± 2.40 µg/cm2·hTissue SampleAbdominal skin of Sprague–Dawley ratsPUBMED ID23311648
ID1028Sequenceβ-Ala-HNameL -carnosineNature of peptide or cargoAntioxidantAssayFranz diffusion cell, HPLCTissue permeability~0.5% of applied doseTissue SampleStratum corneum of human breast skinPUBMED ID22890441
ID1029Sequenceβ-Ala-HNameL -carnosineNature of peptide or cargoAntioxidantAssayFranz diffusion cell, HPLCTissue permeability>0.5% of applied doseTissue SampleStratum corneum of human breast skinPUBMED ID22890441
ID1030Sequenceβ-Ala-HNameL -carnosineNature of peptide or cargoAntioxidantAssayFranz diffusion cell, HPLCTissue permeability>1% of applied doseTissue SampleStratum corneum of human breast skinPUBMED ID22890441
ID1031Sequenceβ-Ala-HNameL -carnosineNature of peptide or cargoAntioxidantAssayFranz diffusion cell, HPLCTissue permeability<0.5% of applied doseTissue SampleStratum corneum of human breast skinPUBMED ID22890441
ID1032Sequenceβ-Ala-HNameL -carnosineNature of peptide or cargoAntioxidantAssayFranz diffusion cell, HPLCTissue permeability<0.5% of applied doseTissue SampleStratum corneum of human breast skinPUBMED ID22890441
ID1033Sequenceβ-Ala-HNameL -carnosineNature of peptide or cargoAntioxidantAssayFranz diffusion cell, HPLCTissue permeability>1.5% of applied doseTissue SampleEpidermis of human breast skinPUBMED ID22890441
ID1034Sequenceβ-Ala-HNameL -carnosineNature of peptide or cargoAntioxidantAssayFranz diffusion cell, HPLCTissue permeability~2% of applied doseTissue SampleEpidermis of human breast skinPUBMED ID22890441
ID1035Sequenceβ-Ala-HNameL -carnosineNature of peptide or cargoAntioxidantAssayFranz diffusion cell, HPLCTissue permeability<4% of applied doseTissue SampleEpidermis of human breast skinPUBMED ID22890441
ID1036Sequenceβ-Ala-HNameL -carnosineNature of peptide or cargoAntioxidantAssayFranz diffusion cell, HPLCTissue permeability~0.5% of applied doseTissue SampleEpidermis of human breast skinPUBMED ID22890441
ID1037Sequenceβ-Ala-HNameL -carnosineNature of peptide or cargoAntioxidantAssayFranz diffusion cell, HPLCTissue permeability<1% of applied doseTissue SampleEpidermis of human breast skinPUBMED ID22890441
ID1038Sequenceβ-Ala-HNameL -carnosineNature of peptide or cargoAntioxidantAssayFranz diffusion cell, HPLCTissue permeability>8% of applied doseTissue SampleDermis of human breast skinPUBMED ID22890441
ID1039Sequenceβ-Ala-HNameL -carnosineNature of peptide or cargoAntioxidantAssayFranz diffusion cell, HPLCTissue permeability<4% of applied doseTissue SampleDermis of human breast skinPUBMED ID22890441
ID1040Sequenceβ-Ala-HNameL -carnosineNature of peptide or cargoAntioxidantAssayFranz diffusion cell, HPLCTissue permeability<18% of applied doseTissue SampleDermis of human breast skinPUBMED ID22890441
ID1041Sequenceβ-Ala-HNameL -carnosineNature of peptide or cargoAntioxidantAssayFranz diffusion cell, HPLCTissue permeability~3% of applied doseTissue SampleDermis of human breast skinPUBMED ID22890441
ID1042Sequenceβ-Ala-HNameL -carnosineNature of peptide or cargoAntioxidantAssayFranz diffusion cell, HPLCTissue permeability>8% of applied doseTissue SampleDermis of human breast skinPUBMED ID22890441
ID1076SequenceRRRRRRRRNamePolyarginineNature of peptide or cargoCell penetrating peptideAssayFranz cell systemTissue permeabilityThe SC, epidermal and dermal retention of SP for SP-NLC-R11 was 10.92, 7.02 and 0.82 mg/g of skin, respectively and the SC, epidermal and dermal retention of KP for KP-NLC-R11 was 0.75, 0.44 and 0.17 mg/g of skin, respectivelyTissue SampleSkin from the dorsal surface of hairless ratPUBMED ID22617521
ID1077SequenceGRKKRRQRRRPPQRKCNameTatNature of peptide or cargoCell penetrating peptideAssayVertical Franz diffusion cell, HPLCTissue permeabilityCumulative amounts 0.20 ± 0.05 mg/cm2 and fluxes 0.20 ± 0.05 mg/cm2·hTissue SampleViable epidermis and dermis (VED) abdominal skin of Sprague Dawley (SD) ratsPUBMED ID22564052
ID1078SequenceGRKKRRQRRRPPQRKCNameTatNature of peptide or cargoCell penetrating peptideAssayVertical Franz diffusion cell, HPLCTissue permeabilityCumulative amounts 0.43 ± 0.04 mg/cm2 and fluxes 0.14 ± 0.01 mg/cm2·hTissue SampleViable epidermis and dermis (VED) abdominal skin of Sprague Dawley (SD) ratsPUBMED ID22564052
ID1079SequenceGRKKRRQRRRPPQRKCNameTatNature of peptide or cargoCell penetrating peptideAssayVertical Franz diffusion cell, HPLCTissue permeabilityCumulative amounts 0.59 ± 0.12 mg/cm2 and fluxes 0.10 ± 0.02 mg/cm2·hTissue SampleViable epidermis and dermis (VED) abdominal skin of Sprague Dawley (SD) ratsPUBMED ID22564052
ID1080SequenceCSNLSTCVLGKLSQELH
KLQTYPRTNTGSGTP
NamesCTNature of peptide or cargoCell penetrating peptideAssayVertical Franz diffusion cell, HPLCTissue permeabilityCumulative amounts 0.67 ± 0.10 mg/cm2 and fluxes 0.67 ± 0.10 mg/cm2·hTissue SampleViable epidermis and dermis (VED) abdominal skin of Sprague Dawley (SD) ratsPUBMED ID22564052
ID1081SequenceCSNLSTCVLGKLSQELH
KLQTYPRTNTGSGTP
NamesCTNature of peptide or cargoCell penetrating peptideAssayVertical Franz diffusion cell, HPLCTissue permeabilityCumulative amounts 0.33 ± 0.09 mg/cm2 and fluxes 0.11 ± 0.03 mg/cm2·hTissue SampleViable epidermis and dermis (VED) abdominal skin of Sprague Dawley (SD) ratsPUBMED ID22564052
ID1082SequenceCSNLSTCVLGKLSQELH
KLQTYPRTNTGSGTP
NamesCTNature of peptide or cargoCell penetrating peptideAssayVertical Franz diffusion cell, HPLCTissue permeabilityCumulative amounts 0.26 ± 0.02 mg/cm2 and fluxes 0.04 ± 0.00 mg/cm2·hTissue SampleViable epidermis and dermis (VED) abdominal skin of Sprague Dawley (SD) ratsPUBMED ID22564052
ID1083SequenceRQIKIWFQNRRMKWKKNamePenetratin (PEN)Nature of peptide or cargoPenetrate through cell and nucleus membranesAssayFranz diffusion cell system, HPLC with photodiode array detectorTissue permeability2-fold higherTissue SamplePorcine ear skinPUBMED ID22306174