PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
16343875-1	2006	The aim of this study was to design site specific, controlled release tablets of N-acetyl-d-glucosamine (NAG), maltose monohydrate and maltopentaose by using hydrophobic matrix formers starch acetate (SA) and ethyl cellulose (EC).	starch acetate	185-199	N-acetyl-alpha-glucosaminidase	Homo sapiens	105-108	
16343875-1	2006	The aim of this study was to design site specific, controlled release tablets of N-acetyl-d-glucosamine (NAG), maltose monohydrate and maltopentaose by using hydrophobic matrix formers starch acetate (SA) and ethyl cellulose (EC).	starch acetate	201-203	N-acetyl-alpha-glucosaminidase	Homo sapiens	105-108	
17075868-1	2007	In this study three model drugs (N-acetyl-D-glucosamine (NAG), anhydrous caffeine, and propranolol hydrochloride) were agglomerated with starch acetate (SA) by mixing the binary powders on a stainless steel (SS) plate.	starch acetate	137-151	N-acetyl-alpha-glucosaminidase	Homo sapiens	57-60