PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
32035254-4	2020	The self-assembly of STC with Soluplus to load FLDP and the microstructure of the SHNPs were confirmed using molecular simulation, STC determination by HPLC and transmission electron microscope.	polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer	30-38	stanniocalcin 1	Homo sapiens	21-24
32035254-4	2020	The self-assembly of STC with Soluplus to load FLDP and the microstructure of the SHNPs were confirmed using molecular simulation, STC determination by HPLC and transmission electron microscope.	polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer	30-38	stanniocalcin 1	Homo sapiens	131-134
32035254-5	2020	Results showed that STC was integrated with Soluplus on the surface of nanoparticles by hydrophobic interactions.	polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer	44-52	stanniocalcin 1	Homo sapiens	20-23
32035254-6	2020	The permeability of FLDP loaded STC/Soluplus SHNPs was STC dependent in the ileum, which was inhibited by the higher concentrations of STC and the inhibitor of apical sodium-dependent bile acid transporter (ASBT).	polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer	36-44	stanniocalcin 1	Homo sapiens	55-58
32035254-6	2020	The permeability of FLDP loaded STC/Soluplus SHNPs was STC dependent in the ileum, which was inhibited by the higher concentrations of STC and the inhibitor of apical sodium-dependent bile acid transporter (ASBT).	polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer	36-44	stanniocalcin 1	Homo sapiens	55-58
32035254-6	2020	The permeability of FLDP loaded STC/Soluplus SHNPs was STC dependent in the ileum, which was inhibited by the higher concentrations of STC and the inhibitor of apical sodium-dependent bile acid transporter (ASBT).	polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer	36-44	solute carrier family 10 member 2	Homo sapiens	160-205
32035254-6	2020	The permeability of FLDP loaded STC/Soluplus SHNPs was STC dependent in the ileum, which was inhibited by the higher concentrations of STC and the inhibitor of apical sodium-dependent bile acid transporter (ASBT).	polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer	36-44	solute carrier family 10 member 2	Homo sapiens	207-211
32035254-7	2020	STC/Soluplus (1:9) SHNPs significantly improved the drug loading of FLDP, achieved the highest permeability of FLDP and realized 1.6-fold of the area under the curve (AUC) of Soluplus self-assembled nanoparticles (SNPs).	polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer	4-12	stanniocalcin 1	Homo sapiens	0-3
32035254-7	2020	STC/Soluplus (1:9) SHNPs significantly improved the drug loading of FLDP, achieved the highest permeability of FLDP and realized 1.6-fold of the area under the curve (AUC) of Soluplus self-assembled nanoparticles (SNPs).	polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer	175-183	stanniocalcin 1	Homo sapiens	0-3
32035254-9	2020	In conclusion, STC/Soluplus SHNPs via ASBT are a potential strategy for enhancing the oral bioavailability of poorly water-soluble drugs.	polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer	19-27	stanniocalcin 1	Homo sapiens	15-18
32035254-9	2020	In conclusion, STC/Soluplus SHNPs via ASBT are a potential strategy for enhancing the oral bioavailability of poorly water-soluble drugs.	polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer	19-27	solute carrier family 10 member 2	Homo sapiens	38-42
27208440-5	2016	Cellular uptake efficiency of HACE/SP NC was higher than that of SP NC, mainly based on HA-CD44 receptor interaction, in MDA-MB-231 (CD44 receptor-positive human breast cancer) cells.	polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer	35-37	CD44 molecule (Indian blood group)	Homo sapiens	91-95
27208440-5	2016	Cellular uptake efficiency of HACE/SP NC was higher than that of SP NC, mainly based on HA-CD44 receptor interaction, in MDA-MB-231 (CD44 receptor-positive human breast cancer) cells.	polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer	35-37	CD44 molecule (Indian blood group)	Homo sapiens	133-137
27208440-8	2016	Given that these experimental results, developed HACE/SP NC can be a promising theranostic nanosystem for CD44 receptor-expressed cancers.	polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer	54-56	CD44 molecule (Indian blood group)	Homo sapiens	106-110