Abstract
Rose hips differ from other fruits with their high vitamin C, vitamin E, phenolic, and antioxidant content, making it an economical source of antioxidants. Exploring the fruit and seed components of different Rosa species could enable better use of their potential for various industries. Thus, rose hips of Rosa corymbifera, Rosa rugosa (Thunb.), Rosa alba L., and Rosa canina L. cultivated in the same growing conditions were analyzed. Their antioxidant activity and capacity, vitamin C, total carotenoids and phenolics, tocopherols and seed oils, as well as their fatty acid composition were determined. In addition to having highly polyunsaturated fatty acids, R. canina was also found to have noticeably high antioxidant components. In the overall evaluation (both fruit and oil characteristics), R. canina was found to have the most favorable content, while R. rugosa has the most desirable oil characteristics. As a result of the evaluation of fruit (excluding oil), R. corymbifera and R. canina were determined as prominent species. Despite medium level oil content, R. rugosa can be recommended for seed oil uses. R. corymbifera and R. canina are recommended for the food and food supplement industry. Production of rose hip species that contain the remarkable functional components of fruits and the health-promoting fatty acids of seeds may be used in combination as a marketing tool. In this way, the medicinal plant market share and profitability rate of rose hip will increase.
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Introduction
In Turkey, rose species grow naturally, and it was only in the last few years that rose hip plants were cultivated on a commercial level. In fact, Rosa canina L. and Rosa corymbifera Borkh. are mainly used as ornamental plants or rootstocks for other cultivated species and varieties in Turkey.
R. corymbifera is a deciduous shrub plant that can grow to around 3 m. It is in the same taxonomic group as R. canina, and its morphological features are similar to the dog rose (D’Angiolillo et al. 2018). Rosa rugosa (Thunb.) is native to the northern coast of Japan and the Korean Peninsula, and is widely distributed in Northeast China and the northern hemisphere (Bruun 2005). R. rugosa, which is traditionally consumed as fruit juice, tea, jam, and marmalade, is a type of rose hip with high phytochemical and biological potential. R. rugosa seeds (achenes) are an important by-product of rose hip production (Patel 2013). Rosa alba L. is a large, down-curved, and thorny tree or shrub measuring up to 1.8 m in height with excellent velvety white roses that can grow in cold and unsuitable soils (Da Silva et al. 2014; Chaturvedi et al. 2009). R. alba is commonly known as white oil rose. It is widely cultivated in Europe, Asia, North America, and Northwest Africa for both ornamental and medicinal purposes due to the aromatic components in its fragrance (Verma et al. 2020).
Today, interest in the consumption of medicinal plants has increased. In particular, their immune-promoting effect has become even more important due to the COVID-19 epidemic that emerged in 2020 (Heiat et al. 2021; Sytar et al. 2021). The consumption of rose hip products is expected to increase in the future parallel to interest in medicinal plant consumption. The interest in rose hip is related to its pharmacologically effective components, especially its antioxidant components (Al-Yafeai et al. 2018). However, other components that confer functional properties on rose hip should be examined in more detail (Akram et al. 2020). Many studies have reported—depending on the components in rose hip varieties—gastro-protective (Gurbuz et al. 2003), antiulcer (Lattanzio et al. 2011), hepatoprotective, and neuroprotective effects, as well as the ability to reduce the risk of cardiovascular diseases, prevent epithelitis after radiotherapy, antiarthritis, chronic musculoskeletal pain, while anticarcinogenic effects have also been reported (Chrubasik-Hausmann et al. 2014).
Rose hips, which are the fruit of the rose bush (Rosa genus), are valued for their flavor, taste, color, and aroma, in accordance with their recognition as one of richest sources of pro-health compounds. Screening, preservation, and propagation of the most valuable local populations of rose hip are carried out for food, pharmacological, and cosmetic applications (Okatan et al. 2019).
Rose hip is one of the important products in terms of quantity in world production and marketing of organic plants collected from nature (Pećinar et al. 2021). Rose hip plantations, which were rarely seen in the past, are now frequently encountered. Variety is reported to be an effective factor in the components of the rose hip (Nađpal et al. 2016; Shameh et al. 2019). Against this background, it is believed that the correct and suitable species and variety selection are important in newly established rose hip plantations. Rose hip is used for various purposes in the food industry, such as jam, marmalade, fruit juice, dried fruit, etc., as well as in the pharmaceutical industry and the food supplement industry, especially to reduce joint pain and strengthen immunity (Ayati et al. 2018). Therefore, determining the components of rose hip varieties and planning production and marketing according to the specified area of use of these components or the appropriate type of industry can lead to commercially successful results. The aim of this study was to determine some of the components and antioxidant activities of four rose hip species grown under the same growing conditions and with the same cultural practices. Depending on the defined components, some species will be recommended to farmers and producers.
Material and Methods
Material
In this study, rose hips of R. corymbifera, R. rugosa, R. alba, and R. canina cultivated in the rose orchard of the Ataturk Horticultural Central Research Institute, Yalova, Turkey, were used as plant material. Rose hips were hand-harvested when skin color turned a full red color in 2018 and 2019. They were stored at −18 oC until analysis.
A total of 3 g of dried and ground samples were taken and homogenized with 25 mL of pure methanol for 2 min and kept at +4 °C overnight. This was then centrifuged at 10,000 rpm for 20 min in a centrifuge. The supernatant was stored at −20 °C until analysis. These prepared extracts were used for the determination of total phenolic substance content and antioxidant activity, as well as for antioxidant capacity analysis (Apak et al. 2004; Thaipong et al. 2006).
Chemical Analyses
The total phenolic contents were determined using the Folin-Ciocalteu method (Thaipong et al. 2006). Antioxidant activity based on electron transfer was determined with the DPPH (2,2-diphenyl-1-picryl-hydrazyl-hydrate) method (Thaipong et al. 2006). Total phenol content and antioxidant activity were expressed as gallic acid equivalent. Antioxidant capacities were determined using the cupric ion reducing antioxidant capacity (CUPRAC) method and expressed as Trolox equivalent (Apak et al. 2004). The DCPIP (2,6-dichlorophenol indophenol) method was used for ascorbic acid content determination (AOAC 1990). Total sugar contents were determined with the Lane and Eynon method (Ranganan 1991). For seed oil determination, rose hips were cut into quarters and the seeds split with tweezers. The oil content of seeds was determined using a Soxhlet extractor (ISO 1988). Total sugar and seed oil content were expressed as percentages (%). Fatty acid composition of seed oils was determined according to the official method (TFC 2014) using a gas chromatography device. Each fatty acid was reported as a percentage of total fatty acids. Total carotenoid content was determined with a spectrophotometric method (Fascella et al. 2019). The official High-performance liquid chromatography (HPLC) method was used for α‑tocopherol and γ‑tocopherol content determination (FAO 2000).
Fatty Acid Composition Analysis
Quality index (QI), polyunsaturated fatty acids (PUFA), monounsaturated fatty acids (MUFA), saturated fatty acids (SFA), MUFA to PUFA ratio, and iodine number (IN) of seed oils were calculated (Kyriakidis and Katsiloulis 2000).
These formulas are as follows:
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SFA (%) = palmitic acid + stearic acid + arashidic acid + behenic acid
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MUFA (%) = palmitoleic acid + oleic acid + eicosenoic acid
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PUFA (%) = linoleic acid + linolenic acid
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IN = 0.93 × (oleic acid + eicosenoic acid) + 1.35 × (linoleic acid) + 2.62 × (linolenic acid)
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QI = Oleic acid/(palmitic acid + linoleic acid)
All of the analyses were repeated three times for each sample. Research was established according to a two factorial (year and species), completely randomized plot design to determine season and species differences. Statistical analysis was performed with the SAS statistical software package program with 0.05 significance value.
Results and Discussion
The flow chart of the study examining the functional properties of R. corymbifera, R. rugosa, R. alba, and R. canina cultivars grown in Turkey is given in Fig. 1.
Both high vitamin C and high total phenolic content are responsible for the high antioxidative activity of rose hip (Larsen et al. 2003). Vitamin E and carotenoids are also reported to be components that contribute to the antioxidative activity (Gruenwald et al. 2019). Vitamin C and total sugar content of rose hip and oil content of seeds are presented in Table 1. Vitamin C and oil content were reported as variable components in rose hip species (Roman et al. 2013). Ercisli and Esitken (2004) as well as Roman et al. (2013) reported the vitamin C content of rose hip to be between 180 and 965 mg/100 g. Dąbrowska et al. (2019) reported the oil content of rose hip seed to be between 7.5 and 8.8%. The total sugar contents of different rose hip genotypes were reported to be 7.95–16.65% (Bilgin et al. 2020) and 15.32–21.57% (Erogul and Oguz 2018). In this study, the vitamin C and total sugar contents of rose hip were determined to be 573.28–900.65 mg/100 g and 2.05–6.63%, respectively. Oil content of rose hip seeds ranged between 5.89 and 16.19%. In general, the oil content of rose hip seeds was higher than other fruits seeds, but lower than oil seeds such as flax (linseed) and sunflower (Wittkop et al. 2009). This result is in agreement with the results of Erogul and Oguz (2018), Roman et al. (2013), and Bilgin et al. (2020). Species differences had a strong effect on the vitamin C and oil contents of rose hips.
Although rose hips do not have high oil content seeds, their oil is rich in terms of bioactive components such as tocopherols, carotenoids, and sterols, which increase the potential medicinal uses of rose hips (Fromm et al. 2012). The total carotene, α‑tocopherol, and γ‑tocopherol contents of rose hips are presented in Table 2. Total carotenoid contents of different rose hip species were reported as between 1204.5 (R. canina) and 1235.7 (R. sempervirens) by Fascella et al. (2019), and 1072.7 (R. corymbifera) and 1061.7 mg/100 g dry weight (R. micrantha) by Andersson et al. (2011). The authors also indicated the statistically significant differences in carotenoid contents, which were caused by genetic, climatic, and ripening stage. This study found similar results (950.09–1356.71 mg/100 g dry weight) to these researchers.
The tocopherol content of rose hip is reported to mainly consist of α‑tocopherol (~ 88%) and γ‑tocopherol (~ 12%). On the other hand, β‑tocopherol and δ(delta)-tocopherol were reported in trace amounts (Kazaz et al. 2009; Westphal et al. 2018). Total tocopherols were reported for in R. dumalis (10.12 µg/g) and R. pisiformis (17.60 µg/g) by Yoruk et al. (2008). The α‑tocopherol and γ‑tocopherol contents of R. canina rose hip were reported to be 12.4 µmol/100 g and 1.7 µmol/100 g, respectively, by Westphal et al. (2018). Similar results (15.9 µmol/100 g total tocopherol) were also reported for R. canina by Al-Yafeai et al. (2018). In this study, statistically significant differences were not determined between species for α‑tocopherol and γ‑tocopherol contents (p < 0.05). However, cultivation years were found to be important for these contents. The highest carotenoids (1249.17–1356.71 mg/100 g dry weight) were found in R. canina, followed by R.rugosa and R. corymbifera.
Total phenolic content and antioxidant characteristics are presented in Table 3. Total phenolic compounds were 4500 mg gallic acid/100 g (PaunoviĆ et al. 2019) and 1900 mg gallic acid/100 g (Mihaylova et al. 2015). Antioxidant activity was 28.4–56.8 µmol TE/g (Erogul and Oguz 2018), and antioxidant capacity of was 35.53 mmol TE/g dry weigh (Demir et al. 2014). Total phenolic compounds of R. canina and R. pimpinellifolia were reported from the same regions and were not significantly different (Fattahi et al. 2012). However, in this study, statistically significant differences were found between species (p < 0.05). Total phenolic content and antioxidant characters were determined to be lower than reported in the literature, but they are still remarkable compared to other fruits with their high antioxidant characteristics. Functional components such as phenolics and carotenoids are quality indicators of foods (Girón et al. 2019). Thus, the production of foods that have a high content of bioactive components can increase the profits of farmers and producers.
The fatty acid composition of rose hip seed is presented in Table 4. Statistically significant differences were not seen for butyric, palmitic, and arachidic acid contents of rose hip cultivars (p < 0.05). R. rugosa has the highest linolenic acid and R. alba the highest oleic acid content, whereas R. alba has the lowest linoleic acid. Linoleic acid (54.80%) and linolenic acid (23.47%) were reported as the major fatty acids in rose hip seed oil (Turan et al. 2018). In this study, linoleic acid, oleic acid, and linolenic acid were determined as the main fatty acids. Similar to our study results, linoleic acid (36–55%) was reported as the most abundant fatty acid, followed by linolenic (17–27%) and oleic acid (15–22%) (Mannozzi et al. 2020).
R. rugosa and R. canina had a higher PUFA content than others, while R. alba had the highest MUFA content. R. canina had the lowest MUFA/PUFA ratio favorable for health nutrition. Calculated fatty acid characteristics are presented in Table 5. Rose hip oil contains more than 77% PUFA and therefore the oil is susceptible to oxidation (Concha et al. 2006). PUFA, MUFA, and SFA ratios of the R. dumalis (MR-12) were reported as 54.65–57.31%, 37.09–40.31%, and 5.56–5.71%, respectively (Gunes et al. 2017). High omega‑6 and omega‑3 group fatty acids of rose hip seed oil are effective in anti-aging and health promotion (Dąbrowska et al. 2019). R. rugosa has a remarkably low QI, whereas R. alba has the highest. The IN of rose hip oil was reported to be 152–169 (Krist 2020) and 179 (Dąbrowska et al. 2019), which is higher than that found in this study. The higher SFA and lower MUFA and PUFA contents were responsible for this difference.
Conclusion
Rose hips are raw materials used in the cosmetics, medicinal, and food industries. The use of functional components of rosehip species in these industries may provide added value. It is important to produce varieties with characteristics specified to meet the growing interest in and specific expectations on rose hip species. The most commonly commercially used rose hip strain is R. canina. The most important quality parameters in R. corymbifera, R. rugosa, R. alba, and R. canina were compared. Thus, this study evaluated a number of functional characters of R. corymbifera, R. rugosa, R. alba, and R. canina to evaluate their potential. Genetic differences were determined as statistically important factors in rose hips, excluding tocopherol, butyric, palmitic, and arachidic acid content (p < 0.05). In the overall evaluation (both fruit and oil characteristics), R. canina were determined as having the most favorable content, followed by R. corymbifera and R. rugosa, while R. rugosa has the most desirable oil characteristics. In addition to having the fatty acids required in terms of health, R. canina also has noticeably higher antioxidant components. When excluding the evaluation of fatty acid compositions and comparing fruit characteristics, R. corymbifera and R. canina were determined as prominent, while R. rugosa and R. alba lagged behind. Despite medium level oil content, R. rugosa can be recommended for oil uses in the skin care, cosmetic, and dermatology industry. Of the rose hip species, the highest vitamin C was observed in R. corymbifera and R. alba species, and a significant difference to R canina was observed. The highest total phenolics and DPPH antioxidants were seen in R canina, followed very closely by R. corymbifera. Therefore, R. corymbifera and R alba could be recommended as a raw material for vitamin C supplement production; on the other hand, R canina and R. corymbifera could be favorable raw materials for phenol supplement production. The R. Rugosa variety showed the highest activity in terms of CUPRAC antioxidant activity. In addition to the high vitamin C, antioxidant, and phenolic components, rose hips are also an important raw material resource for many sectors, since they have a very valuable fatty acid composition and tocophenol content. As a result of this study, it has been found that the R. corymbifera variety has superior properties in terms of its content, and it is an alternative to the commercial variety R. canina. Use of the rose hips R. corymbifera and R. canina can be recommended for the food, food supplement, and drug industry. The functional components and fatty acid composition can be used in tandem as a marketing tool for rose hip, thereby increasing the profitability rate of rose hip farmers.
References
Akram M, Riaz M, Munir N, Akhter N, Zafar S, Jabeen F, Said Khan F (2020) Chemical constituents, experimental and clinical pharmacology of Rosa damascena: a literature review. J Pharm Pharmacol 72(2):161–174. https://doi.org/10.1111/jphp.13185
Al-Yafeai A, Malarski A, Bohm V (2018) Characterization of carotenoids and vitamin E in R. rugosa and R. canina: Comparative analysis. Food Chem 242:435–442. https://doi.org/10.1016/j.foodchem.2017.09.070
Andersson SC, Rumpunen K, Johansson E, Olsson ME (2011) Carotenoid content and composition in rose hips (Rosa spp.) during ripening, determination of suitable maturity marker and implications for health promoting food product. Food Chem 128(3):689–696. https://doi.org/10.1016/j.foodchem.2011.03.088
AOAC (1990) Official methods of analysis of the Association of Official Analytical Chemists, 15th edn. vol II
Apak R, Guclu K, Ozyurek M, Karademir SE (2004) Novel total antioxidant capacity index for dietary polyphenols and vitamins C and E, using their cupric ion reducing capability in the presence of neocuproine: CUPRAC method. J Agric Food Chem 52(26):7970–7981. https://doi.org/10.1021/jf048741x
Ayati Z, Amiri MS, Ramezani M, Delshad E, Sahebkar A, Emami SA (2018) Phytochemistry, traditional uses and pharmacological profile of rose hip: A review. Curr Pharm Des 24(35):4101–4124. https://doi.org/10.2174/1381612824666181010151849
Bilgin NA, Misirli A, Şen F, Türk B, Yağmur B (2020) Fruit pomological, phytochemical characteristic and mineral content of rosehip genotypes. Int J Food Eng 6(1):18–23. https://doi.org/10.18178/ijfe.6.1.18-23
Bruun HH (2005) Rosa rugosa Thunb. ex Murray. J Ecol 93(2):441–470. https://doi.org/10.1111/j.1365-2745.2005.01002.x
Chaturvedi Y, Singh M, Rao GP, Snehi SK, Raj SK (2009) First report of association of “Candidatus Phytoplasma asteris” (16SrI group) with little leaf disease of rose (Rosa alba L.) in India. Plant Pathol 58:788. https://doi.org/10.1111/j.1365-3059.2009.02058.x
Chrubasik-Hausmann S, Chrubasik C, Neumann E, Müller-Ladner UA (2014) Pilot study on the effectiveness of a rose hip shell powder in patients suffering from chronic musculoskeletal pain. Phytother Res 28(11):1720–1726. https://doi.org/10.1002/ptr.5192
Concha J, Soto C, Chamy R, Zúñiga ME (2006) Effect of rosehip extraction process on oil and defatted meal physicochemical properties. J Am Oil Chem Soc 83(9):771–775. https://doi.org/10.1007/s11746-006-5013-2
Da Silva SF, Cardoso JR, Mendes JV, Pinto MV (2014) Pharmacognostic study of Rosa alba L. Rev Eletrôn FMB 7:136–150
D’Angiolillo F, Mammano M, Fascella G (2018) Pigments, polyphenols and antioxidant activity of leaf extracts from four wild Rose species grown in Sicily. Not Bot Horti Agrobo 46(2):402–409. https://doi.org/10.15835/nbha46211061
Demir N, Yildiz O, Alpaslan M, Hayaloglu AA (2014) Evaluation of volatiles, phenolic compounds and antioxidant activities of rose hip (Rosa L.) fruits in Turkey. LWT Food Sci Technol 57(1):126–133. https://doi.org/10.1016/j.lwt.2013.12.038
Dąbrowska M, Maciejczyk E, Kalemba D (2019) Rose hip seed oil: methods of extraction and chemical composition. Eur J Lipid Sci Technol 121(8):1800440. https://doi.org/10.1002/ejlt.201800440
Ercisli S, Esitken A (2004) Fruit characteristics of native rose hip (Rosa spp.) selections from the Erzurum province of Turkey. N Z J Crop Hortic Sci 32(1):51–53. https://doi.org/10.1080/01140671.2004.9514279
Erogul D, Oguz HI (2018) Determining the physico-chemical characterstics of the rosehip genotypes grown naturally in Adiyaman Province. Erwerbs-Obstbau 60(3):195–201. https://doi.org/10.1007/s10341-017-0358-2
FAO (2000) Commission directive 2000/45/EC of 6 july 2000 establishing community methods of analysis for the determination of vitamin A, vitamin E and tryptophan in feedingstuffs
Fascella G, D’angiolillo F, Mammano MM, Amenta M, Romeo FV, Rapisarda P, Ballistreri G (2019) Bioactive compounds and antioxidant activity of four rose hip species from spontaneous Sicilian flora. Food Chem 289:56–64. https://doi.org/10.1016/j.foodchem.2019.02.127
Fattahi S, Jamei R, Hosseini SS (2012) Antioxidant and antiradical activities of Rosa canina and Rosa pimpinellifolia fruits from West Azerbaijan. Iran J Plant Physiol 4:523–529
Fromm M, Bayha S, Kammerer DR, Carle R (2012) Identification and quantitation of carotenoids and tocopherols in seed oils recovered from different Rosaceae species. J Agric Food Chem 60(43):10733–10742. https://doi.org/10.1021/jf3028446
Girón JM, Santos LEO, Rodriguez-Rodriguez DX (2019) Extraction of total carotenoids from peach palm fruit (Bactris gasipaes) peel by means of ultrasound application and vegetable oil. Dyna 86(209):98–103. https://doi.org/10.15446/dyna.v85n207.74840
Gruenwald J, Uebelhack R, Moré MI (2019) Rosa si-Rose hip pharmacological ingredients and molecular mechanics counteracting osteoarthritis—A systematic review. Phytomedicine 60:152958. https://doi.org/10.1016/j.phymed.2019.152958
Gunes M, Dolek U, Elmastas M, Karagöz F (2017) Effects of harvest times on the fatty acids composition of Rose hip (Rosa sp.) seeds. Turkish J Agric Sci Technol 5(4):321–325. https://doi.org/10.24925/turjaf.v5i4.321-325.1064
Gurbuz I, Ustun O, Yesilada E, Sezik E, Kutsal O (2003) Antiulcerogenic activity of some plants used as folk remedy in Turkey. J Ethnopharmacol 88(1):93–97. https://doi.org/10.1016/S0378-8741(03)00174-0
Heiat M, Hashemi-Aghdam MR, Heiat F, Rastegar Shariat Panahi M, Aghamollaei H, Moosazadeh Moghaddam M, Sahebkar A (2021) Integrative role of traditional and modern technologies to combat COVID-19. Expert Rev Anti Infect Ther 19(1):23–33. https://doi.org/10.1080/14787210.2020.1799784
ISO (1988) International Organization for Standardization, ISO 659, 2nd edn.
Kazaz S, Baydar H, Erbas S (2009) Variations in chemical compositions of Rosa damascena Mill. and Rosa canina L. fruits. Czech J Food Sci 27(3):178–184. https://doi.org/10.17221/5/2009-CJFS
Kyriakidis NB, Katsiloulis T (2000) Calculation of iodine value from measurements of fatty acid methyl esters of some oils: comparison with the relevant American oil chemists society method. J Am Oil Chem Soc 77(12):1235–1238
Krist S (2020) Rose hip oil. In vegetable fats and oils. Springer, Cham, pp 647–650
Larsen E, Kharazmi A, Christensen LP, Christensen SB (2003) An antiinflammatory galactolipid from Rose hip (rosa c anina) that inhibits chemotaxis of human peripheral blood neutrophils in vitro. J Nat Prod 66(7):994–995. https://doi.org/10.1021/np0300636
Lattanzio F, Greco E, Carretta D, Cervellati R, Govoni P, Speroni E (2011) In vivo anti-inflammatory effect of Rosa canina L. extract. J Ethnopharmacol 137(1):880–885. https://doi.org/10.1016/j.jep.2011.07.006
Mannozzi C, Foligni R, Scalise A, Mozzon M (2020) Characterization of lipid substances of rose hip seeds as a potential source of functional components: a review. Italian J Food Sci 32(4):721–733. https://doi.org/10.14674/IJFS.1867
Mihaylova D, Georgieva L, Pavlov A (2015) Antioxidant activity and bioactive compounds of Rosa canina L. herbal preparations. Sci Bull Ser F Biotechnol 19:160–165
Nađpal JD, Lesjak MM, Šibul FS, Anačkov GT, Četojević-Simin DD, Mimica-Dukić NM, Beara IN (2016) Comparative study of biological activities and phytochemical composition of two rose hips and their preserves: Rosa canina L. and Rosa arvensis Huds. Food Chem 192:907–914. https://doi.org/10.1016/j.foodchem.2015.07.089
Okatan V, Colak AM, Guclu SF, Korkmaz N, Sekara A (2019) Local genotypes of dog rose from Interior Aegean region of Turkey as a unique source of pro-health compounds. Bragantia 78(3):397–408
Patel S (2013) Rose hips as complementary and alternative medicine: Overview of the present status and prospects. Med J Nutrition Metab 6(2):89–97. https://doi.org/10.1007/s12349-012-0118-7
Paunović D, Kalušević A, Petrović T, Urošević T, Djinović D, Nedović V, Popović-Djordjević J (2019) Assessment of chemical and antioxidant properties of fresh and dried rosehip (Rosa canina L.). Not Bot Horti Agrobo 47(1):108–113. https://doi.org/10.15835/nbha47111221
Pećinar I, Krstić D, Caruso G, Popović-Djordjević JB (2021) Rapid characterization of hypanthium and seed in wild and cultivated rosehip: application of Raman microscopy combined with multivariate analysis. R Soc open sci 8(3):202064. https://doi.org/10.1098/rsos.202064
Ranganan S (1991) Handbook of analysis and quality control. Lane and Eynon method for total sugar determination. McGraw-Hill, New York, pp 12–15
Roman I, Stănilă A, Stănilă S (2013) Bioactive compounds and antioxidant activity of Rosa canina L. biotypes from spontaneous flora of Transylvania. Chem Cent J 7(1):1–10. https://doi.org/10.1186/1752-153X-7-73
Shameh S, Alirezalu A, Hosseini B, Maleki R (2019) Fruit phytochemical composition and color parameters of 21 accessions of five Rosa species grown in North West Iran. J Sci Food Agric 99:5740–5751. https://doi.org/10.1002/jsfa.9842
Sytar O, Brestic M, Hajihashemi S, Skalicky M, Kubeš J, Lamilla-Tamayo L, Landi M (2021) COVID-19 prophylaxis efforts based on natural antiviral plant extracts and their compounds. Molecules 26(3):727. https://doi.org/10.3390/molecules26030727
TFC (2014) Turkish Food Codex, analysis methods communique of olive oil and pomace oil (2014/53)
Thaipong K, Boonprakob U, Crosby K, Cisneros-Zevallos L, Byrne DH (2006) Comparison of ABTS, DPPH, FRAP, and ORAC assays for estimating antioxidant activity from guava fruits extracts. J Food Comp Anal 19:669–675. https://doi.org/10.1016/j.jfca.2006.01.003
Turan S, Solak R, Kiralan M, Ramadan MF (2018) Bioactive lipids, antiradical activity and stability of rosehip seed oil under thermal and photo-induced oxidation. Grasas y Aceites 69(2):248. https://doi.org/10.3989/gya.1114172
Verma A, Srivastava R, Sonar PK, Yadav R (2020) Traditional, phytochemical, and biological aspects of Rosa Alba L.: a systematic review. Futur J Pharm Sci 6:1–8. https://doi.org/10.1186/s43094-020-00132-z
Westphal A, Schwarzenbolz U, Böhm V (2018) Effects of high pressure processing on bioactive compounds in spinach and rosehip puree. Eur Food Res Technol 244(3):395–407. https://doi.org/10.1007/s00217-017-2964-5
Wittkop B, Snowdon RJ, Friedt W (2009) Status and perspectives of breeding for enhanced yield and quality of oilseed crops for Europe. Euphytica 170(1):131–140. https://doi.org/10.1007/s10681-009-9940-5
Yoruk IH, Turker M, Kazankaya A, Erez ME, Batta P, Celik F (2008) Fatty acid, sugar and vitamin contents in rose hip species. Asian J Chem 20(2):1357–1364
Acknowledgements
This study was supported by the Turkish Ministry of Agriculture and Forestry, General Directorate of Agricultural Research and Policies.
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This work was funded by the Ataturk Horticultural Central Research Institute, Turkey.
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F.G. cultivated, followed the maturation levels of, and harvested the rose hips. S.K. determined the total phenolic and ascorbic acid, as well as total sugar contents, antioxidant activity/capacity, and fatty acid compositions. Y.O. determined the oil content of seeds as well as the total carotenoid, α‑tocopherol, and γ‑tocopherol content of rose hips. All authors participated in the preparation of this paper.
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S. Kayahan, Y. Ozdemir, and F. Gulbag declare that they have no competing interests.
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Kayahan, S., Ozdemir, Y. & Gulbag, F. Functional Compounds and Antioxidant Activity of Rosa Species Grown In Turkey. Erwerbs-Obstbau 65, 1079–1086 (2023). https://doi.org/10.1007/s10341-022-00688-5
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DOI: https://doi.org/10.1007/s10341-022-00688-5