All chemicals used in this research are analytical grade. Monopotassium phosphate (KH ₂PO ₄) and dipotassium phosphate (K ₂HPO ₄) were purchased from Merck (Merck Millipore, Darmstadt, Germany); PC, ethanol, and CaCl ₂ – from Sigma-Aldrich (Sigma Aldrich Chemie GmbH, München, Germany); and methanol and acetic acid – from Fluka (Fluka Chemie GmbH, Buchs, Switzerland). As for the plant sample, wild Ruellia tuberosa L. was collected from the area near Universitas Syiah Kuala in Banda Aceh, Aceh, Indonesia. To study the application of the optical pH sensor on the real sample, dead tilapia fishes were used and purchased from the traditional market in Banda Aceh, Aceh, Indonesia.

The procedure follows a previous report. ¹⁹ Briefly, 200 g fresh R. tuberosa L. was macerated in 85 mL methanol for 24 h at room temperature (32-34°C). The residue was then separated from the filtrate by simple filtration. Finally, ACN was obtained after the solvent was removed from the filtrate by means of steaming at 50°C until the volume reached 50 mL.

The optical pH sensor was constructed by dissolving PC powder into a matrix solution (0.1% w/v) in 100 mL CaCl ₂ 0.1 M solution, heated at 60°C. After the mixture was cooled down, the previously obtained ACN extract (1.503 mg/L) was added to 1.66, 2.49 and 3.33 mL PC matrix solution to produce three different 100 mL ACN/PC solutions with respective ACN concentrations of 0.025, 0.0375 and 0.05 mg/L. A total of 40 μL the ACN/PC solution was dropped onto a polyvinylchloride plastic mold surface with a diameter of 0.8 cm ( Figure 1). The sensor was allowed to dry for 24 h at 4 ^oC. Figure 1.

Fourier Transform Infrared (FTIR) Cary 630 Anti Agilent (Penang, Malaysia) was used to identify the structure and functional groups. The membrane morphology was observed under Zeiss Merlin/Merlin Compact/Supra 55VP Field Emission Scanning Electron (FESEM) (Selangor, Malaysia). Thermal stability of the constructed membrane was analyzed using Shimadzu DTG-60 Thermal Gravimetric Analyzer (Kyoto, Japan) and Differential Scanning Calorimetry (DSC) Shimadzu DSC-60 (Kyoto, Japan). Unless otherwise stated, the conditions for these characterizations followed that of reported work for film specimens. ^{20, 21}

To test its response and evaluate its analytical performance, each sensor was dripped with 30 μL 0.1 M phosphate buffer solution with a variety of pH values ranging from 5.0 to 8.5 with 0.5 interval –the pH values of each phosphate solution on the sensor were checked by pH-meter Thermo Orion Star A2111 (Selangor, Malaysia). The sensor color changed corresponding to the different pH values of the administered buffer solutions. It consequently resulted in the difference of the absorbance that was then measured nm using UV-VIS Spectrophotometer (Shimadzu Uv-mini-1240, Kyoto, Japan) at λ _max = 635, ¹⁶ until the sensitivity value for pH determination was obtained.

The effect of PC concentration was tested based on % weight of PC in CaCl ₂ 0.1 M solution; 0.05, 0.10, and 0.15%. In total, 40 μL of the three different PC solutions containing 0.025 mg/L ACN were casted as previously explained above. Finally, the pH sensor was pipetted with 30 μL phosphate buffer 0.1 M (pH 4-9), and its absorbance was measured.

The optical pH sensor with optimum ACN and PC concentrations was used to test its performance against phosphate and citrate buffers 0.1 M (pH 5.0-8.5) to select which buffer generated the best outcome. To select the optimum buffer concentration (once the best buffer had been chosen; phosphate), the best buffer solution was varied in concentration (0.01, 0.03, and 0.05 M) and used in the optical pH sensor performance with pH ranging from 6-8 following the previously explained procedure. The optimum concentration was selected based on its sensitivity and linearity of the absorbance versus pH plotting curve.

Response time of the optical pH sensor was determined by measuring the optimum absorbance of the pH sensor at a range of 5, 10, 15, 20, 25 and 30 minutes. For reproducibility, the performance was conducted 10 times using ten optical pH sensors. For the determination of the optical pH sensor’s lifetime, the absorbance measurement was carried out after 1, 2, 3, 4, 5, 10, 15 and 20 days after the sensor preparation. All of these studies were conducted under optimum buffer conditions.

The pH values of the tilapia fishes were measured by attaching the sensors onto the fishes' surface for 5 minutes before measuring the absorbance, as explained before. The fish were stored at 4°C and ambient temperature (32-34°C). The pH analysis was carried out every 7, 12, 24, and 48 h of the storage time.

Anthocyanin (ACN) is one of the most important components in the construction of this optical pH sensor other than PC. ACN is obtained from the extract of R. tuberosa L. flower that displays different colors at different acidic or basic pH levels. ^{22, 23} FTIR analysis of the extract showed that the broadening vibrational band with medium intensity at the wavenumber, ranged between 3333 cm ^-1 and 3291 cm ^-1, indicating the presence of free O-H groups ( Figure 2). The presence of the aromatic C=C vibrations at wavelength region 1644 cm ^-1 and 1454 cm ^-1 indicates the typical characteristics of an ACN compound. ²⁴ The vibrations by group C-O were recognized from wavelength range 1111 and 1015 cm ^-1. The FT-IR characterization shows that the ACN is in the form of cyanidin-3-glucoside; similar vibration patterns has been reported previously. ²⁵ Figure 2.

FT-IR characterization on PC displayed typical PC functional groups at wavenumber range of 1000-2000 cm ^-1. Spectral band at 1717 cm ^-1 and 1624 cm ^-1 are assigned to be vibrations of C=O stretching from ester and carboxylate. The presence of other spectral band at 3370 cm ^-1 is assigned to the vibrational absorbance of O–H functional groups. The ether bonds of C–O–C is observed by the presence of the absorbance peaks at 1219 and 1096 cm ^-1. In the case of ACN/PC, free O–H groups from the PC molecule were observed from the overlapping band at 3200-3650 cm ^-1. The other spectral bands at 1630 – 1850 cm ^-1 and 1050 – 1260 cm ^-1 are assigned to carbonyl groups (C=O) and symmetrical ether groups (C–O–C) from glycoside bonds, respectively. ^{26, 27}

TGA/DTGA and DSC profiles of PC membrane

Thermal stability is one of preferable characteristics when it comes to a bio-sensor as it may influence its performance. We conducted thermal gravimetry analysis (TGA) and differential scanning calorimetry (DSC) studies to assess whether the PC membrane has ideal thermal stability. The thermograms of TGA and its derivative (DTGA) and DSC have been presented in Figure 3a and b. At around 58°C, the release of solvent (water) was observed on the TGA and DTGA thermograms ( Figure 3a). The second peak of DTGA suggests thermal degradation with 30% weight loss. ²⁸ A better insight regarding the thermal stability of the PC membrane can be seen in the DSC thermogram. ^{20, 21} Figure 3.

The first endothermic peak that appears in the DSC thermogram ( Figure 3b) agrees with the water content release observed in the TGA. T _onset = 83°C indicates the first observable thermal transition, in which it is assigned to melting temperature. It is because within the temperature range (83-118°C), the decrease in weight does not occur in the TGA thermogram. This finding is in line with a previous report investigating PC powder. ²⁹ The exothermal peak (T _peak = ± 309°C) observed afterward indicates the degradation of the PC polymeric chain. From these data, we can conclude that the PC membrane is thermally stable at room temperature range.

SEM images of PC membrane

SEM images of PC ( Figure 4a) and ACN/PC ( Figure 4b) depict a clear difference of surface morphology between the two. ¹⁷ PC surface has a morphology that is uniform and smooth. With the addition of ACN into the membrane, cracks are shown as the result of the presence of the liquid. A similar phenomenon was observed previously, ³⁰ where the cracks were associated with the presence of water. The surface of ACN/PC membrane was divided into darker and lighter areas. The water contents were gathered in areas with a darker color due to their interactions via hydrogen bond. It further results in the disturbance of compacted PC intramolecular interaction, pushing the molecules to have a dense structure resulting in line-like structures with lighter appearance. This change may lead to poorer sensor performance as a transparent membrane is preferred for optical sensor to allow the UV light passing through the membrane. Figure 4.

The constructed optical pH biosensor based on the ACN derived from R. tuberosa L flower has hydrogel characteristics. The advantage of a hydrogel membrane in an optical system is the quick interaction between analyte and active membrane which in turn will accelerate the response time. ^{17, 31} The PC membrane with the immobilized ACN is transparent, where the color change is sensitive against the pH value ( Figure 5). This optical pH sensor is optimized by means of ACN variation to achieve the best sensitivity, observed by a wide linear range and good linearity. Further characterization is followed by the determination of sensor performance. Figure 5.

Color change of ACN can be affected by several factors such as temperature, pH, light intensity, sugar moiety and different phenolic derivatives. ¹⁷ Due to its solubility in aqueous solution, the color change of ACN is caused by structural transformations of carbon skeleton affected by the levels of H ⁺. Four major anthocyanin skeletons have been reported in the literature at different pH values, namely the red flavylium cation (pH below 2), the blue quinoidal base (pH 8-10), the colorless carbinol pseudo base (pH 3-6), and the colorless chalcone (pH 3-6). ^{32, 33} The effect of ACN concentrations on optical pH sensors response has also been studied and shown ( Table 1 and Figure 6). Table 1.

Concentration (mg/L)	pH range	Sensitivity	R 2
0.025	6-8	0.14 ± 0.03	0.999
0.0375	6-8	0.108 ± 0.05	0.999
0.05	6-8	0.094 ± 0.01	0.995

Figure 6.

The sensitivity of the sensor toward variations in ACN concentrations showed not significantly different, but the absorbance vs pH plot showed an increase in the value of the intercept. This indicates the intensity of the sensor color increases with increasing ACN concentrations. Furthermore, the ACN concentration of 0.025 mg/L will be used to construct the optical pH sensor for the next characterization.

Effect of PC weight towards sensor sensitivity

The weight variation of PC (0.05, 0.1, and 0.15% w/v) was studied to find the best sensor sensitivity. At varied weights, PC was dissolved using CaCl ₂ 0.1 M to construct cross linking between Ca ^{2+ ion} and galacturonate until a pectin solution in the form of gel was produced. ³⁴ The effect of PC weight towards the sensitivity of optical pH sensor has been presented ( Figure 7). The optimal weight percentage of PC was found at 0.1 % w/v. The membrane with 0.1% w/v pectin has a flatter surface thus making it as the most suitable optical sensor. PC membrane with only 0.05% w/v PC possessed a gel like texture due to the excess of water which causes a longer time to form a solid membrane. This phenomenon is quite similar for membrane preparation using a phase inversion method. ^{20, 35, 36} On the other hand, membrane with 0.15% PC is very dense and has a non-homogenous surface which is not preferred for optical pH membrane application. ³⁷ Figure 7.

The performance of an optical pH sensor may be affected by the types and concentration of the buffer. Figure 8 shows that the sensitivity of the sensor with phosphate buffer was 0.0877 with an R-square value of 0.993. On the other hand, the ACN/PC sensor with citrate buffer had a sensitivity of 0.074 (R ² = 0.981). Through physical observation, the ANC in the sensor would display a higher color intensity when in phosphate buffer compared to citrate buffer even in the same pH range. This is due to the lower K _a value of phosphate buffer compared to citrate buffer. Altogether, we conclude that the phosphate buffer contributes to better sensitivity of our pH sensor as opposed to citrate buffer. Therefore, the effect of concentration was studied using the phosphate buffer. Figure 8.

The effect of phosphate buffer concentration towards this sensor’s sensitivity is shown in Figure 9. This pH sensor produces the best sensitivity of 0.1238 (R ² = 0.9989) when the phosphate buffer 0.03 M was used. Meanwhile, the sensitivities of the pH sensor using phosphate buffer with concentrations of 0.05 M and 0.1 M were found lower at 0.072 (R ² = 0.9745) and 0.084 (R ² = 0.9805), respectively. The pH sensor with phosphate buffer 0.03 M gave a more contrast in the color change at different pH levels, in comparison with that of citrate buffer. In comparison to other earlier studies, ^{9, 10} our ACN/PC optical pH sensor has a wider working range of pH. Figure 9.

The response time of this sensor was determined by the required duration (minutes) that the sensor achieves a stable result. Response time was determined at 0, 5, 10, 15, 20, 25, and 30 minutes ( Figure 10). The absorbance increased drastically from the first 5 minutes, indicating a good diffusion of the sample onto the membrane. The increase was later observed at minute 10, but no observable significant change afterward. Therefore, the optimum response time of this optical pH sensor is 10 minutes. Figure 10.

In addition, the reproducibility measurement was conducted on 10 different sensors with the same condition, where the relative standard deviation (RSD) was 9.15. This shows that there is a small difference in the absorbance values obtained from the repetition using new sensors. However, RSD that is below 10% is still acceptable for qualitative measurement. ³⁷

The investigated optical pH sensor had a stable response until the tenth day of storage ( Figure 11). Afterward, the sensor response fell as much as 8.3% from the initial response, in which further decline was observed on the 15 ^th day. At the same time, the %RSD also become poor; increasing as much as 36.61% from its initial state. The decrease in sensor performance after particular days of storing depends on the stability of the anthocyanin in maintaining its color. The lifetime of the optical pH sensor in this study is worse in comparison to that of our previous study, ¹⁷ in which the performance did not drop until the 15 ^th day. However, previously we used the synthetic chromoionophore ETH 5294 (CI); unlike in this study where we used natural anthocyanin that can be considered more sustainable. Furthermore, in this study, the lifetime is better in comparison to our currently reported sensor using ACN from Dioscorea alata L. ³⁷ Figure 11.

Optical pH sensor with the optimal conditions was used to monitor the freshness of tilapia fish that was kept at 4 ^oC. The pH profile of the fish at two conditions, namely room temperature and 4°C storage temperature, is shown in Figure 12. A living fish has a pH value of around 7.4, but after death the pH decreases. ³⁸ The pH of the fish samples was measured after 0, 7, 12, 24 and 48 h storage time at room temperature and 4°C. Fish freshness was measured based on the absorbance value that is converted to pH value based on the constructed calibration curve. Figure 12.

Fish samples kept at room temperature possess a higher pH compared to the fish sample stored at 4°C. Fresh fish that was measured at 0 hours displayed pH of around 7.3-7.4. Following that, the pH decreases to 5.5-5.9, indicating that the fish has reached rigor mortis or postmortem rigidity. After the rigor mortis phase, the fish will undergo putrefaction due to the microbial activity in the fish sample. ³⁹ This activity causes the pH to become more basic due to the breakdown of proteins in the fish sample to become ammonia and trimethylamine. ^{22– 24} Results achieved from pH measurements at 7, 12, 24 and 48 hours at 4°C using the optical sensor yielded results of pH 5.9, 6.9, 7.1 and 7.9. Based on these results, it can be said that fish that is kept at room temperature will undergo a faster decomposition. This is due to the exposure to sunlight thus a higher temperature that will accelerate the process of decomposition.

Harvard Dataverse: Data Set for Optical pH Sensor Based on Pectin and Ruellia tuberosa L-derived Anthocyanin for Fish Freshness Monitoring, https://doi.org/10.7910/DVN/ZYCXAM. ⁴⁰

Data are available under the terms of the Creative Commons Zero “No rights reserved” data waiver (CC0 1.0 Public domain dedication).