Halimium halimifolium : From the Chemical and Functional Characterization to a Nutraceutical Ingredient Design 1

被引:11
作者
Kerbab, Khawla [1 ]
Sansone, Francesca [2 ]
Zaiter, Lahcene [1 ]
Esposito, Tiziana [2 ]
Celano, Rita [2 ]
Franceschelli, Silvia [2 ]
Pecoraro, Michela [2 ]
Benayache, Fadila [1 ]
Rastrelli, Luca [2 ]
Picerno, Patrizia [2 ]
Aquino, Rita P. [2 ]
Mencherini, Teresa [2 ]
机构
[1] Univ Constantine 1, Dept Chim, Fac Sci Exactes, Unite Rech Valorisat Ressources Nat Mol Bioact &, Constantine, Algeria
[2] Univ Salerno, Dept Pharm, Via Giovanni Paolo II 132, I-84084 Fisciano, SA, Italy
关键词
Halimium halimifolium; Cistaceae; antioxidant activity; antihyperglycemic activity; spray drying; gastro-resistant microparticles; nutraceuticals; ALPHA-GLUCOSIDASE; TECHNOLOGICAL PROPERTIES; PHENOLIC-COMPOUNDS; IN-VITRO; FLAVONOIDS; ANTIOXIDANT; MICROPARTICLES; INHIBITION; IDENTIFICATION; COMPOUND;
D O I
10.1055/a-0953-6007
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Halimium halimifolium (Hh) is a shrub used in Algerian folk medicine to treat gastrointestinal pain. An UHPLC-PDA-ESI/MS (n) method was developed to identify the metabolic profile of the traditionally used infusion (Hh-A) from the aerial parts. The structures of flavanols were confirmed by NMR analysis after the isolation procedure from a hydrohalcolic extract (Hh-B) that also allowed for the identification of phenolic acids, an aryl butanol glucoside, and different derivatives of quercetin, myricetin, and kaempferol. Tiliroside isomers were the chemical markers of Hh-A and Hh-B (54.33 and 36.00 mg/g, respectively). Hh-A showed a significant scavenging activity both against the radicals 1,1-diphenyl-2-picrylhydrazyl and 2,2 '-Azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (EC (50) = 10.49 mu g/mL and TEAC value = 1.98 mM Trolox/mg infusion) and the lipopolysaccharide-induced reactive oxygen species release in A375 and HeLa cells. Moreover, the antihyperglycemic properties, by inhibiting the alpha -amylase and alpha -glucosidase enzymes (IC (50) = 0.82 mg/mL and 25.01 mu g/mL, respectively), were demonstrated. To upgrade the therapeutic effect, a microencapsulation process is proposed as a strategy to optimize stability, handling, and delivery of bioactive components, avoiding the degradation and loss of the biological efficacy after oral intake. Hh-loaded microparticles were designed using cellulose acetate phthalate as the enteric coating material and spray drying as a production process. The results showed a satisfactory process yield (67.9%), encapsulation efficiency (96.7%), and micrometric characteristics of microparticles (laser-scattering, fluorescent, and scanning electron microscopy). In vitro dissolution studies (USPII-pH change method) showed that Hh-loaded microparticles are able to prevent the release and degradation of the bioactive components in the gastric tract, releasing them into the intestinal environment.
引用
收藏
页码:1024 / 1033
页数:10
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