Planta Med 2019; 85(11/12): 1024-1033
DOI: 10.1055/a-0953-6007
Biological and Pharmacological Activities
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

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

Khawla Kerbab
1   Unité de recherche Valorisation des Ressources Naturelles, Molécules Bioactives et Analyses Physicochimiques et Biologiques (VARENBIOMOL), Département de Chimie, Faculté des Sciences Exactes, Université Constantine 1, Constantine, Algérie
,
Francesca Sansone
2   Department of Pharmacy, University of Salerno, Fisciano (SA), Italy
,
Lahcene Zaiter
1   Unité de recherche Valorisation des Ressources Naturelles, Molécules Bioactives et Analyses Physicochimiques et Biologiques (VARENBIOMOL), Département de Chimie, Faculté des Sciences Exactes, Université Constantine 1, Constantine, Algérie
,
Tiziana Esposito
2   Department of Pharmacy, University of Salerno, Fisciano (SA), Italy
,
Rita Celano
2   Department of Pharmacy, University of Salerno, Fisciano (SA), Italy
,
Silvia Franceschelli
2   Department of Pharmacy, University of Salerno, Fisciano (SA), Italy
,
Michela Pecoraro
2   Department of Pharmacy, University of Salerno, Fisciano (SA), Italy
,
Fadila Benayache
1   Unité de recherche Valorisation des Ressources Naturelles, Molécules Bioactives et Analyses Physicochimiques et Biologiques (VARENBIOMOL), Département de Chimie, Faculté des Sciences Exactes, Université Constantine 1, Constantine, Algérie
,
Luca Rastrelli
2   Department of Pharmacy, University of Salerno, Fisciano (SA), Italy
,
Patrizia Picerno
2   Department of Pharmacy, University of Salerno, Fisciano (SA), Italy
,
Rita P. Aquino
2   Department of Pharmacy, University of Salerno, Fisciano (SA), Italy
,
Teresa Mencherini
2   Department of Pharmacy, University of Salerno, Fisciano (SA), Italy
› Author Affiliations
Further Information

Publication History

received 22 February 2019
revised 06 June 2019

accepted 07 June 2019

Publication Date:
01 July 2019 (online)

Abstract

Halimium halimifolium (Hh) is a shrub used in Algerian folk medicine to treat gastrointestinal pain. An UHPLC-PDA-ESI/MSn 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) (EC50 = 10.49 µg/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 α-amylase and α-glucosidase enzymes (IC50 = 0.82 mg/mL and 25.01 µg/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.

1 Dedicated to Professor Dr. Cosimo Pizza 70th birthday in recognition of his outstanding contribution to natural product research.


 
  • References

  • 1 Díaz Antunes-Barradas M, Zunzunegui González M, García Novo F. Autoecological notes of Halimium halimifolium at Donana national park. Lagascalia 1997; 19: 725-736
  • 2 Rebaya A, Belghith SI, Hammrouni S, Maaroufi A, Ayadi T, Chérif JK. Antibacterial and antifungal activities of ethanol extracts of Halimium halimifolium, Cistus salviifolius and Cistus monspeliensis . Int J Pharm Clin Res 2016; 8: 243-247
  • 3 Rebaya A, Belghith SI, Baghdikian B, Leddet VM, Mabrouki F. Total phenolic, total flavonoid, tannin content, and antioxidant capacity of Halimium halimifolium (Cistaceae). J Appl Pharm Sci 2015; 5: 52-57
  • 4 Zaiter L, Bouheroum M, Hammoud L, Sarri D, Benayache S, Leon F, Brouard I, Bermejo J. Phytochemical study of Halimium halimifolium . Chem Nat Compd 2012; 47: 889-890
  • 5 Souza PM, Sales PM, Simeoni LA, Silva EC, Silveira D, Magalhães Pde O. Inhibitory activity of α-amylase and α-glucosidase by plant extracts from the Brazilian cerrado. Planta Med 2012; 78: 393-399
  • 6 Rios JL, Francini F, Schinella GR. Natural products for the treatment of type 2 diabetes mellitus. Planta Med 2015; 81: 975-994
  • 7 Afifi-Yazar FU, Kasabri V, Abu-Dahab R. Medicinal plants from Jordan in the treatment of diabetes: traditional uses vs. in vitro and in vivo evaluations–part 2. Planta Med 2011; 77: 1210-1220
  • 8 Proenca C, Freitas M, Ribeiro D, Oliveira EFT, Sousa JLC, Tom SM, Ramos MJ, Silva AMS, Fernandes PA, Fernandes E. α-Glucosidase inhibition by flavonoids: an in vitro and in silico structure-activity relationship study. J Enzyme Inhib Med Chem 2017; 32: 1216-1228
  • 9 Lo Piparo E, Scheib H, Frei N, Williamson G, Grigorov M, Chou CJ. Flavonoids for controlling starch digestion: structural requirements for inhibiting human r-amylase. J Med Chem 2008; 51: 3555-3561
  • 10 Del Gaudio P, De Cicco F, Sansone F, Aquino RP, Adami R, Ricci M, Giovagnoli S. Alginate beads as a carrier for omeprazole/SBA-15 inclusion compound: A step towards the development of personalized paediatric dosage forms. Carbohydr Polym 2015; 133: 464-472
  • 11 Puccetti M, Giovagnoli S, Zelante T, Romani L, Ricci M. Development of novel indole-3-aldehyde-loaded gastro-resistant spray-dried microparticles for postbiotic small intestine local delivery. J Pharm Sci 2018; 107: 2341-2353
  • 12 Sansone F, Rossi A, Del Gaudio P, De Simone F, Aquino RP, Lauro MR. Hesperidin gastroresistant microparticles by spray-drying: preparation, characterization, and dissolution profiles. AAPS PharmSciTech 2009; 10: 391-401
  • 13 Lauro MR, De Simone F, Sansone F, Iannelli P, Aquino RP. Preparations and release characteristics of naringin and naringenin gastro-resistant microparticles by spray-drying. J Drug Deliv Sci Tec 2007; 17: 119-124
  • 14 Sansone F, Mencherini T, Picerno P, DʼAmore M, Aquino RP, Lauro MR. Maltodextrin/pectin microparticles by spray drying as carrier for nutraceutical extracts. J Food Eng 2011; 105: 468-476
  • 15 Oliveira GF, Ferrari PC, Carvalho LQ, Evangelista RC. Chitosan–pectin multiparticulate systems associated with enteric polymers for colonic drug delivery. Carbohydr Polym 2010; 82: 1004-1009
  • 16 Sansone F, Esposito T, Lauro MR, Picerno P, Mencherini T, Gasparri F, De Santis S, Chieppa M, Cirillo C, Aquino RP. Application of spray drying particle engineering to a extract: powders production and characterization. Molecules 2018; 23: 1-17
  • 17 Del Gaudio P, Auriemma G, Russo P, Mencherini T, Campiglia P, Stigliani M, Aquino RP. Novel co-axial prilling technique for the development of core-shell particles as delayed drug delivery systems. Eur J Pharm Biopharm 2014; 87: 541-547
  • 18 Jablan J, Jug M. Development of Eudragit® S100 based pH-responsive microspheres of zaleplon by spray-drying: Tailoring the drug release properties. Powder Technol 2015; 283: 334-343
  • 19 Lin LZ, Harnly JM. A screening method for the identification of glycosylated flavonoids and other phenolic compounds using a standard analytical approach for all plant materials. J Agric Food Chem 2007; 55: 1084-1096
  • 20 Gutzeit D, Wray V, Winterhalter P, Jerz G. Preparative isolation and purification of flavonoids and protocatechuic acid from sea buckthorn juice concentrate (Hippophaë rhamnoides L. ssp. rhamnoides) by high-speed counter-current chromatography. Chromatographia 2007; 65: 1-7
  • 21 Cho J, Moon J, Seong K, Park K. Antimicrobial activity of 4-hydroxybenzoic acid and trans 4-hydroxycinnamic acid isolated and identified from rice hull. Biosci Biotechnol Biochem 1998; 62: 2273-2276
  • 22 Ooshiro A, Hiradate S, Kawano S, Takushi T, Fujii Y, Natsume M, Abe H. Identification and activity of ethyl gallate as an antimicrobial compound produced by Geranium carolinianum . Weed Biol Manag 2009; 9: 169-172
  • 23 Yim S, Lee YJ, Park KD, Lee I, Shin BA, Jung D, Williams DR, Kim HJ. Phenolic constituents from the flowers of Hamamelis japonica Sieb. et Zucc. Nat Prod Sci 2015; 21: 162-169
  • 24 Itoh T, Ninomiya M, Yasuda M, Koshikawa K, Deyashiki Y. Inhibitory effects of flavonoids isolated from Fragaria ananassa Duch on IgE-mediated degranulation in rat basophilic leukemia RBL-2H3. Bioorg Med Chem 2009; 17: 5374-5379
  • 25 Rashed K, Calland N, Deloison G, Rouillé Y, Séron K. In-vitro antiviral activity of Pistacia chinensis flavonoids against hepatitis C virus (HCV). J Appl Pharm 2014; 6: 8-18
  • 26 Alves CQ, David JM, David JP, Villareal CF, Soares MBP, de Queiroz LP, Aguiar RM. Flavonoids and other bioactive phenolics isolated from Cenostigma macrophyllum (Leguminosae). Quim Nova 2012; 35: 1137-1140
  • 27 Li H, Song H, Li H, Pan Y, Li R. Characterization of phenolic compounds from Rhododendron alutaceum . Arch Pharm Res 2012; 35: 1887-1893
  • 28 Mansour A, Celano R, Mencherini T, Picerno P, Piccinelli AL, Foudil-Cherif Y, Csupor D, Rahili G, Yahi N, Nabavi SM, Aquino RP, Rastrelli L. A new cineol derivative, polyphenols and norterpenoids from Saharan myrtle tea (Myrtus nivellei): Isolation, structure determination, quantitative determination and antioxidant activity. Fitoterapia 2017; 119: 32-39
  • 29 Xu X, Xie H, Hao J, Jiang Y, Wei X. Flavonoid glycosides from the seeds of Litchi chinensis . J Agric Food Chem 2011; 59: 1205-1209
  • 30 Grochowski DM, Locatelli M, Granica S, Cacciagrano F, Tomczyk M. A review on the dietary flavonoid tiliroside. Compr Rev Food Sci Food Saf 2018; 17: 1395-1421
  • 31 Kim Y, Keogh JB, Clifton PM. Polyphenols and glycemic control. Nutrients 2016; 8: E17
  • 32 Tsao R. Chemistry and biochemistry of dietary polyphenols. Nutrients 2010; 2: 1231-1246
  • 33 Rubilar M, Jara C, Poo Y, Acevedo F, Gutierrez C, Sineiro J, Shene C. Extracts of Maqui (Aristotelia chilensis) and Murta (Ugni molinae Turcz): Sources of antioxidant compounds and α-Glucosidase/α-Amylase inhibitors. J Agric Food Chem 2011; 59: 1630-1637
  • 34 Clifford MN. Diet-derived phenols in plasma and tissues and their implications for health. Planta Med 2004; 70: 1103-1114
  • 35 Sansone F, Mencherini T, Picerno P, Esposito T, Del Gaudio P, Russo P, Pepe G, Lauro MR, Aquino RP. Microencapsulation by spray drying of Lannea microcarpa extract: Technological characteristics and antioxidant activity. J Pharm Pharmacogn Res 2014; 2: 100-109
  • 36 Sansone F, Picerno P, Mencherini T, Porta A, Lauro MR, Russo P, Aquino RP. Technological properties and enhancement of antifungal activity of a Paeonia rockii extract encapsulated in a chitosan-based matrix. J Food Eng 2014; 120: 260-267
  • 37 Esposito T, Sansone F, Franceschelli S, Del Gaudio P, Picerno P, Aquino RP, Mencherini T. Hazelnut (Corylus avellana L.) shells extract: Phenolic composition, antioxidant effect and cytotoxic activity on human cancer cell lines. Int J Mol Sci 2017; 18: 392-404
  • 38 Piccinelli AL, Pagano I, Esposito T, Mencherini T, Porta A, Petrone AM, Gazzerro P, Picerno P, Sansone F, Rastrelli L, Aquino RP. HRMS profile of a hazelnut skin proanthocyanidin-rich fraction with antioxidant and anti-Candida albicans activities. J Agric Food Chem 2016; 64: 585-595
  • 39 Esposito T, Celano R, Pane C, Piccinelli AL, Sansone F, Picerno P, Zaccardelli M, Aquino RP, Mencherini T. Chestnut (Castanea sativa Miller.) burs extracts and functional compounds: UHPLC-UV-HRMS profiling, antioxidant activity, and inhibitory effects on phytopathogenic fungi. Molecules 2019; 24: E302
  • 40 Adesso S, Pepe G, Sommella E, Scopa A, Sofo A, Tenore C, Gaudio D, Autore G, Marzocco S. Anti-inflammatory and antioxidant activity of polyphenolic extracts from Lactuca sativa (var. Maravilla de Verano) under different farming methods. J Sci Food Agric 2016; 96: 4194-4206
  • 41 Pecoraro M, Pinto A, Popolo A. Inhibition of Connexin 43 translocation on mitochondria accelerates CoCl 2-induced apoptotic response in a chemical model of hypoxia. Toxicol In Vitro 2018; 47: 120-128
  • 42 Tadera KT, Minami YM, Takamatsu KT, Matsuoka TM. Inhibition of α-glucosidase and α-amylase by flavonoids. J Nutr Sci Vitaminol 2006; 52: 149-153
  • 43 Saltos BMV, Puente NFB, Faraone I, Milella L, De Tommasi N, Braca A. Inhibitors of α-amylase and α-glucosidase from Andromachia igniaria . Phytochem Lett 2015; 14: 45-50
  • 44 Del Gaudio P, Sansone F, Mencherini T, De Cicco F, Russo P, Aquino RP. Nanospray drying as a novel tool to improve technological properties of soy isoflavone extracts. Planta Med 2017; 83: 426-433